P. Moerman

发表

Potential Targets' Analysis Reveals Dual PI3K/mTOR Pathway Inhibition as a Promising Therapeutic Strategy for Uterine Leiomyosarcomas—an ENITEC Group Initiative

E. Wardelmann, K. K. van de Vijver, M. Zikan, 2017, Clinical Cancer Research.

Recurrent copy number alterations in BRCA1‐mutated ovarian tumors alter biological pathways

B. De Moor, O. Gevaert, A. Daemen, 2009, Human mutation.

Prognostic implications of lobular breast cancer histology: new insights from a single hospital cross-sectional study and SEER data.

P. Neven, M. Christiaens, H. Wildiers, 2014, Breast.

Ovarian cancer arising in endometrioid cysts: ultrasound findings

D. Timmerman, G. Scambia, G. Ferrandina, 2011, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

External Validation of Mathematical Models to Distinguish Between Benign and Malignant Adnexal Tumors: A Multicenter Study by the International Ovarian Tumor Analysis Group

Sabine Van Huffel, Dirk Timmerman, Enrico Ferrazzi, 2007, Clinical Cancer Research.

Imaging of gynecological disease (3): clinical and ultrasound characteristics of granulosa cell tumors of the ovary

D. Jurkovic, D. Timmerman, L. Valentin, 2008, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Fetal heart pathology on postmortem 3‐T magnetic resonance imaging

S. Dymarkowski, L. Fedele, J. Deprest, 2014, Prenatal diagnosis.

The use of laser microdissection and SELDI-TOF MS in ovarian cancer tissue to identify protein profiles.

B. De Moor, A. Daemen, R. Zeillinger, 2009, Anticancer research.

Presymptomatic Identification of Cancers in Pregnant Women During Noninvasive Prenatal Testing.

P. Neven, J. Vermeesch, L. Dehaspe, 2015, JAMA oncology.

Fetal akinesia deformation sequence: a study of 30 consecutive in utero diagnoses.

J. Fryns, P. Moerman, I. Witters, 2002, American journal of medical genetics.

Upregulation of Wilms' tumour gene 1 (WT1) in uterine sarcomas.

F. Amant, A. Coosemans, G. Verbist, 2007, European journal of cancer.

Endometrial carcinosarcomas have a different prognosis and pattern of spread compared to high-risk epithelial endometrial cancer.

P. Neven, I. Vergote, F. Amant, 2005, Gynecologic oncology.

Endometrial stromal sarcoma with a sole t(X;17) chromosome change: report of a case and review of the literature.

A. Hagemeijer, M. Debiec‐Rychter, F. Amant, 2003, Gynecologic oncology.

Transition of epithelial toward mesenchymal differentiation during ovarian carcinosarcoma tumorigenesis.

F. Amant, P. Moerman, I. Vergote, 2003, Gynecologic oncology.

Sentinel lymph node involvement in ductal carcinoma in-situ of the breast: two different causes.

P. Neven, R. Paridaens, M. Christiaens, 2012, Clinical breast cancer.

Ovarian borderline mucinous tumor in a premenarchal girl: review on ovarian epithelial cancer in young girls.

J. Deprest, P. Moerman, P. Ide, 1992, Gynecologic oncology.

CASE REPORT Ovarian Borderline Mutinous Tumor in a Premenarchal Girl: Review on Ovarian Epithelial Cancer in Young Girls

J. Deprest, P. Moerman, P. Ide, 1992 .

Does estrogen receptor negative/progesterone receptor positive breast carcinoma exist?

E. van Limbergen, N. Pochet, P. Neven, 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Detection and diagnosis

P. Neven, C. Denkert, M. Dietel, 2012 .

In-vitro adhesion of endometrium to autologous peritoneal membranes: effect of the cycle phase and the stage of endometriosis.

P. Moerman, T. D’Hooghe, S. Debrock, 2002, Human reproduction.

The prognostic role of preoperative and (early) postoperatively change in CA15.3 serum levels in a single hospital cohort of primary operable breast cancers.

P. Neven, M. Christiaens, H. Wildiers, 2013, Breast.

A thin and regular endometrium on ultrasound is very unlikely in patients with endometrial malignancy

D. Timmerman, T. Van den Bosch, F. Amant, 2007, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The pedicle artery sign based on sonography with color Doppler imaging can replace second‐stage tests in women with abnormal vaginal bleeding

S. Huffel, D. Timmerman, S. Van Huffel, 2003, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Neuropathological findings in Moebius syndrome

R. Dom, J. Fryns, P. Moerman, 1998, Clinical genetics.

First trimester prenatal diagnosis of 13q‐syndrome presenting with increased nuchal translucency, Dandy‐Walker malformation and small parietal encephalocoele

H. Van Esch, R. Devlieger, J. Fryns, 2008, Prenatal diagnosis.

Proteomic analysis of laser microdissected ovarian cancer tissue with SELDI-TOF MS.

P. Moerman, T. Van Gorp, E. Waelkens, 2011, Methods in molecular biology.

Diffusely Metastasized Adenocarcinoma Arising in a Mucinous Carcinoid of the Ovary: A Case Report.

I. Vergote, P. Moerman, A. Vanderstichele, 2017, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

Staging with Unilateral Salpingo-Oophorectomy and Expert Pathological Review Result in No Recurrences in a Series of 81 Intestinal-Type Mucinous Borderline Ovarian Tumors

P. Neven, F. Amant, P. Moerman, 2017, Gynecologic and Obstetric Investigation.

Fetal akinesia sequence caused by nemaline myopathy.

R. Dom, J. Fryns, P. Moerman, 1997, Neuropediatrics.

Body mass index, age at breast cancer diagnosis, and breast cancer subtype: a cross-sectional study

P. Neven, R. Paridaens, H. Wildiers, 2018, Breast Cancer Research and Treatment.

Identification of a novel, recurrent MBTD1‐CXorf67 fusion in low‐grade endometrial stromal sarcoma

R. Sciot, M. Debiec‐Rychter, F. Amant, 2014, International journal of cancer.

Regulation of insulin-like growth factor-I and insulin-like growth factor binding protein-1 concentrations in preterm fetuses.

L. Giudice, J. Verhaeghe, P. Moerman, 2003, American journal of obstetrics and gynecology.

The Use of Lymph Vessel Markers to Predict Endometrial Cancer Outcome

F. Amant, B. Calster, G. Verbist, 2010, International Journal of Gynecologic Cancer.

Testicular histology in boys with Prader-Willi syndrome: fertile or infertile?

P. Moerman, G. Bogaert, A. Vogels, 2008, The Journal of urology.

Congenital pulmonary lymphangiectasis with chylothorax: a heterogeneous lymphatic vessel abnormality.

J. Fryns, P. Moerman, H. Devlieger, 1993, American journal of medical genetics.

Prophylactic salpingo-oophorectomy in 51 women with familial breast–ovarian cancer: importance of fallopian tube dysplasia

P. Neven, F. Amant, E. Legius, 2005, International Journal of Gynecologic Cancer.

The fetal akinesia deformation sequence. A fetopathological approach.

J. Fryns, P. Moerman, 1990, Genetic counseling.

Fetal akinesia sequence caused by glycogenosis type VII.

J. Fryns, P. Moerman, M. Lammens, 1995, Genetic counseling.

Marden—Walker syndrome versus isolated distal arthrogryposis: Evidence that both conditions may be variable manifestations of the same mutated gene

J. Fryns, P. Moerman, D. Schoubroeck, 1998, Clinical genetics.

Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: further evidence for autosomal recessive inheritance of hydranencephaly, fowler type.

K. Devriendt, J. Fryns, P. Moerman, 2002, American journal of medical genetics.

Diaphragmatic hernia in Denys-Drash syndrome.

K. Devriendt, F. de Zegher, E. Legius, 1995, American journal of medical genetics.

In early-stage breast cancer, the estrogen receptor interacts with correlation between human epidermal growth factor receptor 2 status and age at diagnosis, tumor grade, and lymph node involvement.

B. van Calster, V. Van Belle, P. Neven, 2008, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Para-aortic lymph node metastases in locally advanced cervical cancer: Comparison between surgical staging and imaging.

E. van Limbergen, F. Amant, P. Moerman, 2015, Gynecologic oncology.

Multiple ankyloses, facial anomalies, and pulmonary hypoplasia associated with severe antenatal spinal muscular atrophy.

J. Fryns, P. Moerman, J. Lauweryns, 1983, Jornal de Pediatria.

Establishment and characterization of uterine sarcoma and carcinosarcoma patient-derived xenograft models.

D. Lambrechts, F. Amant, Tine Cuppens, 2017, Gynecologic oncology.

Pathogenesis of the prune-belly syndrome: a functional urethral obstruction caused by prostatic hypoplasia.

J. Fryns, P. Moerman, J. Lauweryns, 1984, Pediatrics.

The diaphragm of the newborn infant: anatomical and ultrasonographic studies.

G. Marchal, P. Moerman, P. Casaer, 1991, Journal of developmental physiology.

Localisation of breast lesions with MR mammography (work-in-progress)

H. Bosmans, M. Christiaens, A. Baert, 1995, European Radiology.

Meigs' syndrome with elevated serum CA 125 levels: two case reports and review of the literature.

D. Timmerman, I. Vergote, P. Moerman, 1995, Gynecologic oncology.

The Role of Adjuvant Chemotherapy in Surgical Stages I-II Serous and Clear Cell Carcinomas and Carcinosarcoma of the Endometrium: A Collaborative Study

P. Neven, F. Amant, J. Trovik, 2010, International Journal of Gynecologic Cancer.

Idiopathic infantile arterial calcification with cardiac, renal and central nervous system involvement

G. Marchal, P. Moerman, W. Proesmans, 2004, European Journal of Pediatrics.

Late‐Onset visceral presentation with cardiomyopathy and without neurological symptoms of adult Sanfilippo A syndrome

R. Sciot, G. Matthijs, R. Wevers, 2003, American journal of medical genetics. Part A.

ERBB-2 gene overexpression and amplification in uterine sarcomas.

I. Vergote, M. Debiec‐Rychter, F. Amant, 2004, Gynecologic oncology.

Nonimmunologic hydrops fetalis. A study of ten cases.

J. Fryns, P. Moerman, J. Lauweryns, 1982, Archives of pathology & laboratory medicine.

Primary invasive mucinous ovarian carcinoma of the intestinal type: importance of the expansile versus infiltrative type in predicting recurrence and lymph node metastases.

P. Neven, F. Amant, P. Moerman, 2013, European journal of cancer.

Immunological response after WT1 mRNA-loaded dendritic cell immunotherapy in ovarian carcinoma and carcinosarcoma.

F. Amant, Z. Berneman, A. Coosemans, 2013, Anticancer research.

The pathology of trisomy 13 syndrome

J. Fryns, P. Moerman, J. Lauweryns, 1988, Human Genetics.

A morphometric study of the human fetal heart on post‐mortem 3‐tesla magnetic resonance imaging

L. Fedele, J. Deprest, P. Moerman, 2013, Prenatal diagnosis.

Acceptance, reliability and confidence of diagnosis of fetal and neonatal virtuopsy compared with conventional autopsy: a prospective study

J. de Mey, P. Moerman, J. Jani, 2012, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Short-Term Prognostic Index for Breast Cancer: NPI or Lpi

S. Huffel, V. Van Belle, P. Neven, 2007, Pathology research international.

Coexistence of Gaucher disease type 1 and Joubert syndrome

P. Moerman, 2022 .

Suggestively increased rate of infant death in children of fra(X) positive mothers.

J. Fryns, P. Moerman, H. van den Berghe, 1988, American journal of medical genetics.

Net‐targeted mutant mice develop a vascular phenotype and up‐regulate egr‐1

K. Alitalo, B. Wasylyk, H. Zheng, 2001, The EMBO journal.

Adenoid cystic carcinoma arising in an adenomyoepithelioma of the breast

P. Moerman, J. Dorpe, J. van Dorpe, 1998, Virchows Archiv.

Prenatal diagnosis of MPPH syndrome

H. Van Esch, P. Moerman, L. de Catte, 2013, Prenatal diagnosis.

Pseudomyxoma peritonei associated with a mucinous ovarian tumor arising from a mature cystic teratoma. A case report.

F. Amant, P. Moerman, I. Vergote, 2006, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

Clinical study investigating the role of lymphadenectomy, surgical castration and adjuvant hormonal treatment in endometrial stromal sarcoma

B. van Calster, P. Neven, S. Van Huffel, 2007, British Journal of Cancer.

Lung metastasis of malignant epithelioid hemangioendothelioma mimicking a primary intravascular bronchioalveolar tumor. A histologic, ultrastructural, and immunohistochemical study

P. Moerman, E. Verbeken, D. Knockaert, 1985, Cancer.

Is there a role for neoadjuvant chemotherapy in the treatment of stage IV serous endometrial carcinoma?

F. Amant, P. Moerman, I. Vergote, 2005, International Journal of Gynecologic Cancer.

Hereditary hydronephrosis and the short arm of chromosome 6

J. Fryns, P. Moerman, K. Vandenberghe, 1993, Human Genetics.

Kit Gene in Endometrial Carcinoma: An Immunohistochemical and Mutational Analysis

M. Debiec‐Rychter, F. Amant, G. Verbist, 2011, International Journal of Gynecologic Cancer.

Fertility Preservation Is Safe for Serous Borderline Ovarian Tumors

P. Neven, F. Amant, P. Moerman, 2016, International Journal of Gynecologic Cancer.

Genomic Characterisation and Response to Trastuzumab and Paclitaxel in Advanced or Recurrent HER2-positive Endometrial Carcinoma.

D. Lambrechts, F. Amant, Tine Cuppens, 2016, Anticancer research.

Amplification and expression of the HMGIC gene in a benign endometrial polyp

A. D. Dei Tos, G. Tallini, P. Moerman, 1998, Genes, chromosomes & cancer.

The addition of 4% oxygen to the CO(2) pneumoperitoneum does not decrease dramatically port site metastases.

F. Amant, P. Moerman, I. Vergote, 2008, Journal of minimally invasive gynecology.

Fetal Magnetic Resonance Imaging of an Intracranial Venous Thrombosis

M. Smet, L. Breysem, P. Moerman, 2005, Fetal Diagnosis and Therapy.

Successful conservative treatment of endocervical adenocarcinoma stage Ib1 diagnosed early in pregnancy

I. Vergote, F. Amant, P. Moerman, 2008, Acta obstetricia et gynecologica Scandinavica.

Homozygous loss-of-function mutation in ALMS1 causes the lethal disorder mitogenic cardiomyopathy in two siblings.

H. Peeters, K. Devriendt, A. Corveleyn, 2014, European journal of medical genetics.

Presence and course of the incisive canal in the human mandibular interforaminal region: two-dimensional imaging versus anatomical observations

M. Quirynen, R. Jacobs, D. Steenberghe, 2003, Surgical and Radiologic Anatomy.

Sedaghatian Type of Spondylometaphyseal Dysplasia and Concurrent Anomalies

P. Moerman, L. Catte, I. Witters, 2009 .

Endometrial cancer.

Patrick Neven, Dirk Timmerman, Philippe Moerman, 2005, Lancet.

Intra-uterine Candida infection: a report of four infected fetusses from two mothers.

P. Moerman, G. Donders, F. V. Van Assche, 1991, European journal of obstetrics, gynecology, and reproductive biology.

Pathogenesis of the lethal multiple pterygium syndrome.

J. Fryns, A. Cornelis, P. Moerman, 1990, American journal of medical genetics.

Lymphangiomatosis of the body wall: a report of two cases associated with chylothorax and fatal outcome.

P. Moerman, C. Van Geet, H. Devlieger, 1997, Pediatric pathology & laboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association.

Idiopathic granulomatous mastitis

C. Van Ongeval, A. Baert, P. Moerman, 1997, European Radiology.

Importance of pathological review of gestational trophoblastic diseases: results of the Belgian Gestational Trophoblastic Diseases Registry

P. Delvenne, E. Marbaix, P. Moerman, 2022, International Journal of Gynecological Cancer.

Pregnancy outcome and long term prognosis in 868 children born after second trimester amniocentesis for maternal serum positive triple test screening and normal prenatal karyotype

K. Devriendt, J. Fryns, E. Legius, 2001, Journal of medical genetics.

Human Chorionic Gonadotropin Regression Curves after Partial or Complete Molar Pregnancy in Flanders: Are They Different from Regression Curves from the Eighties?

I. Vergote, P. Moerman, Sileny N. Han, 2017, Gynecologic and Obstetric Investigation.

[Belgian register and reference centers for gestational trophoblastic diseases].

P. Delvenne, M. Timmermans, I. Vergote, 2015, Revue medicale de Liege.

Endodermal sinus tumor of the vulva: successfully treated with high-dose chemotherapy.

I. Vergote, P. Moerman, J. Maertens, 2004, International journal of gynecological cancer : official journal of the International Gynecological Cancer Society.

Endodermal sinus tumor of the vulva: successfully treated with high-dose chemotherapy

I. Vergote, P. Moerman, J. Maertens, 2004, International Journal of Gynecologic Cancer.

Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome.

B. Migeon, J. Fryns, P. Moerman, 2001, Annales de genetique.

Caudal developmental field defect with female pseudohermaphroditism and VACTERL anomalies.

J. Fryns, P. Moerman, T. Lukusa, 1996, Genetic counseling.

5q- anomaly in a patient with disseminated teratoma.

G. Tricot, J. Fryns, P. Moerman, 1983, Cancer genetics and cytogenetics.

Anaplastic nodules in an ovarian mucinous tumor. Case report and literature review.

D. Timmerman, I. Vergote, P. Moerman, 1998, European journal of gynaecological oncology.

The genetic landscape of 87 ovarian germ cell tumors.

P. Neven, D. Lambrechts, I. Vergote, 2018, Gynecologic oncology.

Positive maternal serum triple test screening in severe early onset hypophosphatasia

J. Fryns, P. Moerman, E. Mornet, 2004, Prenatal diagnosis.

Male Wolffian adnexal tumor: the first report of long-term follow-up after radical surgical treatment

P. Moerman, S. Joniau, R. De vos, 2021, Current urology.

Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins

Kristin M. Scheible, U. Surti, P. Stankiewicz, 2016, Human Genetics.

A new lethal chondrodysplasia with spondylocostal dysostosis, multiple internal anomalies and Dandy‐Walker cyst

J. Fryns, P. Moerman, K. Vandenberghe, 1985, Clinical genetics.

Integrated genome analysis of uterine leiomyosarcoma to identify novel driver genes and targetable pathways

D. Lambrechts, M. Zikan, F. Amant, 2018, International journal of cancer.

Constrictive amniotic bands, amniotic adhesions, and limb-body wall complex: discrete disruption sequences with pathogenetic overlap.

J. Fryns, P. Moerman, K. Vandenberghe, 1992, American journal of medical genetics.

Association of Meckel syndrome with M‐anisosplenia in one patient

J. Fryns, P. Moerman, J. Lauweryns, 1982, Clinical genetics.

Cystic hygroma colli as the first echographic sign of the fetal akinesia sequence.

J. Fryns, P. Moerman, F. V. Van Assche, 2001, Genetic counseling.

Early onset asymmetrical intrauterine growth retardation with fetal hypokinesia and variable expression of acral and genitourinary malformations: a new lethal MCA syndrome

J. Fryns, P. Moerman, F. V. Van Assche, 2003, Journal of medical genetics.

Popliteal pterygium and multiple pterygium syndromes.

J. Fryns, P. Moerman, 2001, American journal of medical genetics.

Cystic hygroma and multiple pterygium syndrome.

J. Fryns, P. Moerman, H. van den Berghe, 1984, Annales de genetique.

The echographic diagnosis of fetal akinesia. A challenge towards etiological diagnosis and management.

W. Gyselaers, J. Fryns, P. Moerman, 1990, Genetic counseling.

Hereditary renal adysplasia: new observations and hypotheses.

J. Fryns, P. Moerman, K. Vandenberghe, 1994, Pediatric pathology.

The fetal phenotype in 15q2 duplication.

J. Fryns, P. Moerman, H. van den Berghe, 1988, Annales de genetique.

Evolution in Endometrial Cancer: Evidence From an Immunohistochemical Study

L. Akslen, F. Amant, J. Trovik, 2011, International Journal of Gynecologic Cancer.

Characterization of patient-derived tumor xenograft models of endometrial cancer for preclinical evaluation of targeted therapies.

D. Lambrechts, F. Amant, D. Annibali, 2015, Gynecologic oncology.

Chromosome 22q11 deletion presenting as the Potter sequence.

K. Devriendt, J. Fryns, P. Moerman, 1997, Journal of medical genetics.

Chorangiocarcinoma of the placenta: a case report and clinical review.

P. Moerman, A. Pecceu, T. Faes, 2012, Placenta.

Somatic copy number alterations predict response to platinum therapy in epithelial ovarian cancer.

D. Lambrechts, R. Zeillinger, F. Amant, 2014, Gynecologic oncology.

Somaticcopynumberalterations predictresponsetoplatinumtherapyin epithelial ovarian cancer

D. Lambrechts, J. Sehouli, P. Moerman, 2014 .

Second case of uterine mesonephric adenocarcinoma.

I. Vergote, F. Amant, P. Moerman, 2006, International Journal of Gynecological Cancer.

Clinicopathologic markers of uterine leiomyosarcoma originating from smooth muscle tumors of low malignancy

I. Vergote, G. Tulunay, M. Debiec‐Rychter, 2005 .

A new cytogenetic subgroup in uterine leiomyoma is characterized by a deletion of the long arm of chromosome 3

P. Cin, J. Deprest, P. Moerman, 1995, Genes, chromosomes & cancer.

Observation of a deletion of the long arm of chromosome 6 in benign fibrocystic disease of the breast constitutes a challenging problem

M. Christiaens, P. Moerman, H. van den Berghe, 1996, Genes, chromosomes & cancer.

Pseudomyxoma Peritonei Originating from an Intestinal Duplication

R. Sciot, P. Moerman, A. D'Hoore, 2013, Case reports in pathology.

Mesonephric (Wolffian) Pseudoendometrioid Carcinoma of the Broad Ligament, Arising From a Papillary Cystadenoma

F. Amant, P. Moerman, I. Vergote, 2016, International journal of surgical pathology.

Mesonephric Carcinoma of the Ovary: A Report of Two Cases

I. Vergote, P. Moerman, Eveline Lurquin, 2015 .

Second case of uterine mesonephric adenocarcinoma

F. Amant, P. Moerman, I. Vergote, 2005, International Journal of Gynecologic Cancer.

Triple negative breast cancer: clinical characteristics in the different histological subtypes.

B. van Calster, P. Neven, R. Paridaens, 2013, Breast.

Endometrial carcinosarcoma with osteoclast-like giant cells.

F. Amant, P. Moerman, T. Van Gorp, 2006, European journal of gynaecological oncology.

Pulmonary sequestration: a comparison between pediatric and adult patients.

P. Moerman, G. Deneffe, T. Lerut, 2001, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

The classification of a uterine sarcoma as 'high-grade endometrial stromal sarcoma' should be abandoned.

F. Amant, P. Moerman, I. Vergote, 2004, Gynecologic oncology.

THE DIAGNOSTIC PROBLEM OF ENDOMETRIAL STROMAL SARCOMA: REPORT ON SIX CASES

P. Neven, F. Amant, P. Moerman, 2003, International Journal of Gynecologic Cancer.

Neoadjuvant chemotherapy followed by radical hysterectomy for invasive cervical cancer diagnosed during pregnancy: report of a case and review of the literature

L. Lagae, I. Vergote, F. Amant, 2004, International Journal of Gynecologic Cancer.

Report of an unusual problematic uterine smooth muscle neoplasm, emphasizing the prognostic importance of coagulative tumor cell necrosis

I. Vergote, F. Amant, P. Moerman, 2004, International Journal of Gynecologic Cancer.

Pitfall in the diagnosis of endometrial cancer: case report of an endometrioid adenocarcinoma arising from uterine adenomyosis.

D. Timmerman, F. Amant, P. Moerman, 2011, European journal of gynaecological oncology.

First‐trimester scan in trisomy 14 mosaicism

J. Fryns, P. Moerman, I. Witters, 2004, Prenatal diagnosis.

Double autosomal trisomy (1q21.2----qter and 14pter----q13) in a female fetus with nuchal oedema.

J. Fryns, P. Moerman, H. van den Berghe, 1987, Annales de genetique.

Neoadjuvant chemotherapy followed by large cone resection as fertility-sparing therapy in stage IB cervical cancer.

E. van Limbergen, P. Neven, P. Moerman, 2015, Gynecologic oncology.

Diaphragmatic hernia with extralobar lung sequestration in the Beckwith-Wiedemann syndrome.

J. Fryns, P. Moerman, L. Witters, 2004, Genetic counseling.

Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic congenital diaphragmatic hernia.

K. Devriendt, J. Vermeesch, J. Deprest, 2014, European journal of medical genetics.

Scalp defects in Fryns syndrome.

J. Fryns, P. Moerman, 1998, Genetic counseling.

The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome.

J. Opitz, J. Fryns, P. Moerman, 1988, American journal of medical genetics.

Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndrome.

J. Fryns, P. Moerman, P. Petit, 1992, American journal of medical genetics.

Absence of correlation between risk factors for endometrial cancer and the presence of tamoxifen-associated endometrial polyps in postmenopausal patients with breast cancer.

D. Timmerman, I. Vergote, J. Deprest, 2000, European journal of cancer.

The diagnostic problem of endometrial stromal sarcoma

P. Neven, F. Amant, P. Moerman, 2002 .

Hyperreactio luteinalis in a spontaneously conceived singleton pregnancy

D. Timmerman, F. Amant, P. Moerman, 2009, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Liver necrosis in the new-born infant: Analysis of some precipitating factors in neonatal care

P. Moerman, H. Devlieger, E. Eggermont, 1982, European Journal of Pediatrics.

Congenital eventration of the diaphragm: an unusual cause of intractable neonatal respiratory distress with variable etiology.

J. Opitz, J. Fryns, P. Moerman, 1987, American journal of medical genetics.

X-linked centronuclear myopathy as a cause of floppy baby.

P. Moerman, H. Devlieger, B. Spitz, 1987, European journal of obstetrics, gynecology, and reproductive biology.

Qualitative assessment of the progesterone receptor and HER2 improves the Nottingham Prognostic Index up to 5 years after breast cancer diagnosis.

B. van Calster, V. Van Belle, P. Neven, 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Loss of 1p36.33 Frequent in Low-Grade Serous Ovarian Cancer

P. Neven, D. Lambrechts, P. Moerman, 2019, Neoplasia.

Neonatal transthoracic puncture in a case of congenital cystic adenomatoid malformation of the lung.

P. Moerman, G. Naulaers, M. Proesmans, 2002, Journal of pediatric surgery.

Tracheal bronchus associated with congenital cystic adenomatoid malformation

P. Moerman, T. Lerut, D. Van raemdonck, 1995, Pediatric pulmonology.

Pathogenesis of congenital cystic adenomatoid malformation of the lung

J. Fryns, P. Moerman, H. Devlieger, 1992, Histopathology.

Associated malformations and chromosomal anomalies in 42 cases of prenatally diagnosed diaphragmatic hernia.

D. Timmerman, J. Deprest, J. Fryns, 2001, American journal of medical genetics.

Bilateral tibial agenesis with ectrodactyly (OMIM 119100): further evidence for autosomal recessive inheritance.

K. Devriendt, J. Fryns, P. Moerman, 2001, American journal of medical genetics.

Severe primary pulmonary hypoplasia ("acinar dysplasia") in sibs: a genetically determined mesodermal defect?

J. Fryns, P. Moerman, H. Devlieger, 1998, Journal of medical genetics.

Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?

J. Fryns, P. Moerman, C. D. de Die-Smulders, 1999, Journal of Medical Genetics.

46,XY/46,XX mosaicism and congenital pulmonary lymphangiectasis with chylothorax.

J. Fryns, P. Moerman, 1993, American journal of medical genetics.

Prenatal echographic diagnosis of laryngeal atresia as part of a multiple congenital anomalies (MCA) syndrome.

J. Fryns, P. Moerman, I. Witters, 2000, Genetic counseling.

Prenatal diagnosis and pulmonary pathology in congenital high airway obstruction sequence

J. Fryns, P. Moerman, L. de Catte, 2009, Prenatal diagnosis.

Diaphragmatic hernia in the Coffin-Siris syndrome.

J. Fryns, P. Moerman, V. Delvaux, 1998, Genetic counseling.

Laryngeal atresia sequence as part of the DiGeorge developmental field defect.

F. de Zegher, J. Fryns, P. Moerman, 1992, Genetic counseling.

Intractable asphyxia at birth: analysis of the underlying conditions.

P. Moerman, P. Casaer, H. Devlieger, 1994, European journal of obstetrics, gynecology, and reproductive biology.

Proceedings of the International Cancer Imaging Society (ICIS) 16th Annual Teaching Course

Jeong Min Lee, W. Oyen, J. Fütterer, 2016, Cancer Imaging.

Right diaphragmatic eventration associated with intralobar pulmonary sequestration: a case report.

P. Moerman, G. Naulaers, H. Devlieger, 2000, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Tetraphocomelia and bilateral femorotibial synostosis. A severe variant of the thrombocytopenia-absent radii (TAR) syndrome?

J. Fryns, P. Moerman, K. van den Berghe, 1992, Genetic counseling.

The Roberts tetraphocomelia syndrome: identical limb defects in two siblings.

J. Fryns, P. Moerman, H. van den Berghe, 1987, Annales de genetique.

Abnormal lung features on prenatal ultrasound and postnatal outcome

R. Devlieger, L. Breysem, P. Moerman, 2010 .

Type III congenital cystic adenomatoid malformation of the lung: another cause of elevated alpha fetoprotein?

J. Fryns, P. Moerman, H. Berghe, 1987, Clinical genetics.

Acceptance, reliability and confidence of diagnosis of fetal and neonatal virtuopsy compared with conventional autopsy: a prospective study

Kees van Berkel, J. de Mey, P. Moerman, 2012, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes

T. Mazza, H. Van Esch, H. Kayserili, 2016, Journal of Medical Genetics.

Neonatal haemochromatosis

P. Pauwels, J. Fryns, P. Moerman, 1990, Histopathology.

Termination of pregnancy for renal malformations

P. Moerman, F. Claus, A. Hindryckx, 2015, Pediatric Nephrology.

The Meckel syndrome. Pathological and cytogenetic observations in eight cases

J. Fryns, P. Moerman, E. Verbeken, 2004, Human Genetics.

Spectrum of clinical and autopsy findings in trisomy 18 syndrome.

J. Fryns, P. Moerman, J. Lauweryns, 1982, Journal de genetique humaine.

Endometrial cancer

Patrick Neven, Dirk Timmerman, Philippe Moerman, 2005, The Lancet.

Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5)(p13.1 → p15.3)

J. Fryns, P. Moerman, H. Berghe, 1987, Clinical genetics.

High-throughput interrogation of PIK3CA, PTEN, KRAS, FBXW7 and TP53 mutations in primary endometrial carcinoma.

A. Spurdle, D. Lambrechts, J. Marcickiewicz, 2013, Gynecologic oncology.

New models to predict depth of infiltration in endometrial carcinoma based on transvaginal sonography

N. Pochet, B. De Moor, D. Timmerman, 2006, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Neoadjuvant chemotherapy followed by interval debulking surgery in patients with serous endometrial cancer with transperitoneal spread (stage IV): a new preferred treatment?

B. van Calster, P. Neven, F. Amant, 2009, British Journal of Cancer.

Applying the 2011 St Gallen panel of prognostic markers on a large single hospital cohort of consecutively treated primary operable breast cancers.

E. van Limbergen, P. Neven, R. Paridaens, 2012, Annals of oncology : official journal of the European Society for Medical Oncology.

Triple negative breast cancer: a study from the point of view of basal CK5/6 and HER-1

V. Van Belle, P. Neven, V. Belle, 2009, Journal of Clinical Pathology.

Triple-negative breast cancer

R. Paridaens, H. Wildiers, P. Moerman, 2008, Current opinion in oncology.

Treatment modalities in endometrial cancer

E. van Limbergen, D. Timmerman, P. Neven, 2007, Current opinion in oncology.

Epithelial Ovarian Cancer: Rationale for Changing the One-Fits-All Standard Treatment Regimen to Subtype-Specific Treatment

E. Berns, D. Lambrechts, F. Amant, 2014, International Journal of Gynecologic Cancer.

Wilms' tumor gene 1 (WT1) in endometrial carcinoma.

P. Neven, F. Amant, A. Coosemans, 2008, Gynecologic oncology.

Lobular and non-lobular breast cancers differ regarding axillary lymph node metastasis: a cross-sectional study on 4,292 consecutive patients

S. Huffel, P. Neven, M. Christiaens, 2011, Breast Cancer Research and Treatment.

Neoadjuvant Weekly Paclitaxel-Carboplatin Is Effective in Stage I–II Cervical Cancer

P. Neven, F. Amant, P. Moerman, 2017, International Journal of Gynecologic Cancer.

Wilms' Tumor Gene 1 (WT1)--loaded dendritic cell immunotherapy in patients with uterine tumors: a phase I/II clinical trial.

F. Amant, Z. Berneman, A. Coosemans, 2013, Anticancer research.

Wilms Tumor Gene 1 (WT1) is a Prognostic Marker in High-Grade Uterine Sarcoma

B. van Calster, F. Amant, A. Coosemans, 2010, International Journal of Gynecologic Cancer.

Short limbed dwarfism, genital hypoplasia, sparse hair, and vertebral anomalies: a variant of Ellis-van Creveld syndrome?

J. Fryns, P. Moerman, 1993, Journal of medical genetics.

Numerical Chromosome Aberrations in Fibrothecoma

P. Moerman, H. van den Berghe, P. Dal Cin, 1992, Tumori.

Goldston syndrome reconsidered.

P. Pauwels, J. Fryns, P. Moerman, 1993, Genetic Counseling.

Partial trisomy 3p/monosomy 9p with sex reversal

P. Moerman, J. Fryns, I. Witters, 2004, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father Clinical variability of 22q11 deletion

K. Devriendt, J. Fryns, P. Moerman, 1997, Clinical genetics.

Partial duplications of the ATRX gene cause the ATR-X syndrome

K. Devriendt, J. Vermeesch, B. Thienpont, 2007, European Journal of Human Genetics.

Immunohistochemical expression of CD10 antigen in uterine adenosarcoma

V. Abeler, G. Tulunay, F. Amant, 2004, International Journal of Gynecologic Cancer.

Primitive neuroectodermal tumor: a newly recognized cause of early fetal death.

J. Fryns, P. Moerman, J. Lauweryns, 1985, Pediatric pathology.

Congenital muscular dystrophy associated with lethal arthrogryposis multiplex congenita

J. Fryns, P. Moerman, J. Lauweryns, 2004, Virchows Archiv A.

MCA syndrome with renal-hepatic-pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and Müllerian duct anomalies.

K. Devriendt, J. Fryns, P. Moerman, 2002, American journal of medical genetics.

Oligomeganephronic renal hypoplasia in two siblings.

P. Moerman, B. van Damme, H. Devlieger, 1984, The Journal of pediatrics.

Thrombosis of the right umbilical artery, presumably related to the shortness of the umbilical cord: an unusual cause of fetal distress.

P. Moerman, H. Devlieger, E. Eggermont, 1983, European journal of obstetrics, gynecology, and reproductive biology.

Primary Retroperitoneal Mucinous Cystadenocarcinoma: A Case Report and Review of the Literature

F. Amant, P. Moerman, V. Schelfhout, 2010, Gynecologic and Obstetric Investigation.

The fetal phenotype of partial trisomy of the long arm of chromosome 4 (4q22----4qter).

J. Fryns, P. Moerman, P. Petit, 1991, Genetic Counseling.

Symmetrical tetraphocomelia without associated congenital malformations: a nosological dilemma.

J. Fryns, P. Moerman, I. Witters, 2002, American journal of medical genetics.

The more you look, the more you find: challenging results on FDG-PET CT in a patient with neurofibromatosis type I

Patrick Schöffski, Christophe M. Deroose, Olivier Gheysens, 2014, BMC Medical Imaging.

Uterine Carcinosarcoma With Melanocytic Differentiation

F. Amant, P. Moerman, I. Vergote, 2001, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

Expression of ERCC1, p53, and Class III &bgr;-Tubulin Do Not Reveal Chemoresistance in Endometrial Cancer: Results From an Immunohistochemical Study

F. Amant, G. Verbist, P. Moerman, 2011, International Journal of Gynecologic Cancer.

Immunohistochemical determination of estrogen and progesterone receptor positivity in uterine adenosarcoma.

V. Abeler, I. Vergote, G. Tulunay, 2004, Gynecologic oncology.

CA 125 concentrations in ovarian 'chocolate' cyst fluid can differentiate an endometriotic cyst from a cystic corpus luteum.

J. Deprest, P. Moerman, C. Meuleman, 1992, Human reproduction.

Whole-body MRI with diffusion-weighted sequence for staging of patients with suspected ovarian cancer: a clinical feasibility study in comparison to CT and FDG-PET/CT

S. Dymarkowski, F. Amant, P. Moerman, 2014, European Radiology.

Ovarian borderline mucinous tumor in a premenarchal girl: Review on ovarian epithelial cancer in young girls

J. Deprest, P. Moerman, P. Ide, 1993 .

Aberrant twinning (diprosopus) associated with anencephaly

J. Fryns, P. Moerman, A. Assche, 1983, Clinical genetics.

Different patterns of pulmonary sequelae after hyaline membrane disease: heterogeneity of bronchopulmonary dysplasia? A clinicopathologic study.

A. Cornelis, P. Moerman, H. Devlieger, 1991, Biology of the neonate.

HPV induced ovarian squamous cell carcinoma: case report and review of the literature

F. Amant, P. Moerman, I. Vergote, 2007, Archives of Gynecology and Obstetrics.

Unknown syndrome: abnormal facies, hypothyroidism, and severe retardation: a second patient.

J. Fryns, P. Moerman, 1988, Journal of medical genetics.

Prenatal Diagnosis of Smith–Lemli–Opitz Syndrome

J. Fryns, P. Moerman, M. Cannie, 2008 .

Post‐zygotic origin of isochromosome 12p

T. de Ravel, J. Vermeesch, J. Fryns, 2004, Prenatal diagnosis.

Prenatal ultrasound diagnosis of rhizomelic chondrodysplasia punctata in a primigravida

J. Fryns, P. Moerman, K. Vandenberghe, 1994, Prenatal diagnosis.

Predictors of axillary lymph node metastases in early breast cancer and their applicability in clinical practice.

P. Neven, R. Paridaens, M. Christiaens, 2013, Breast.

Metastatic renal cell carcinoma presenting as a breast mass in a woman with history of primary breast cancer.

M. Christiaens, C. Van Ongeval, P. Moerman, 2011, JBR-BTR : organe de la Societe royale belge de radiologie (SRBR) = orgaan van de Koninklijke Belgische Vereniging voor Radiologie.

Subcapsular hemorrhage of the liver and hemoperitoneum in premature infants: report of 4 cases.

F. de Zegher, P. Moerman, H. Devlieger, 1992, European journal of obstetrics, gynecology, and reproductive biology.

Semilobar holoprosencephaly in a 46,XY female fetus

K. Devriendt, J. Fryns, M. Muenke, 2001, Prenatal diagnosis.

Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observation.

J. Fryns, E. Legius, P. Moerman, 1988, American journal of medical genetics.

Prediction of non-sentinel lymph node involvement in breast cancer patients with a positive sentinel lymph node.

P. Neven, P. V. van Dam, M. Christiaens, 2014, Breast.

Are gene signatures better than traditional clinical factors?

V. Van Belle, P. Neven, R. Paridaens, 2008, The Lancet. Oncology.

Papillary adenocarcinoma of the prostatic urethra.

P. Moerman, R. Vereecken, S. Witters, 1986, European Urology.

Skeletal dysplasias: 38 prenatal cases.

J. Fryns, P. Moerman, I. Witters, 2008, Genetic counseling.

Case report of a poorly differentiated uterine tumour with t(10;17) translocation and neuroectodermal phenotype.

M. Debiec‐Rychter, F. Amant, P. Moerman, 2011, Anticancer research.

Mutation profile and clinical outcome of mixed endometrioid-serous endometrial carcinomas are different from that of pure endometrioid or serous carcinomas

D. Lambrechts, M. Zikan, F. Amant, 2015, Virchows Archiv.

Diagnostic value of whole body diffusion-weighted MRI compared to computed tomography for pre-operative assessment of patients suspected for ovarian cancer.

F. De Keyzer, F. Amant, R. Vanslembrouck, 2017, European journal of cancer.

Vulvar ulcers: a differential diagnosis between Behçet’s disease and Lipschütz ulcus

F. Amant, P. Moerman, P. Koninckx, 2007 .

Wilms’ tumour gene 1 (WT1) positivity in endothelial cells surrounding epithelial uterine tumours

P. Neven, F. Amant, L. Moons, 2009, Histopathology.

Hamartoma of the breast with involvement of 6p21 and rearrangement of HMGIY

M. Christiaens, P. Moerman, H. van den Berghe, 1997, Genes, chromosomes & cancer.

Decidual vasculopathy and extensive placental infarction in a patient with repeated thromboembolic accidents, recurrent fetal loss, and a lupus anticoagulant.

J. Vermylen, P. Moerman, F. de Wolf, 1982, American Journal of Obstetrics and Gynecology.

Whole-body diffusion-weighted magnetic resonance imaging in the diagnosis of recurrent ovarian cancer: a clinical feasibility study.

F. De Keyzer, F. Amant, R. Vanslembrouck, 2016, British Journal of Radiology.

Breast cancer phenotype, nodal status and palpability may be useful in the detection of overdiagnosed screening-detected breast cancers.

E. van Limbergen, P. Neven, E. Kellen, 2013, Annals of oncology : official journal of the European Society for Medical Oncology.

CD10, estrogen and progesterone receptor expression in ovarian adenosarcoma.

V. Abeler, F. Amant, T. van Mieghem, 2005, Gynecologic oncology.

Immunohistochemical determination of hormone receptors in uterine adenosarcomas.

F. Amant, P. Moerman, I. Vergote, 2003, Gynecologic Oncology.

Heterogeneity in omphalocoele with absent radial ray complex.

K. Devriendt, J. Fryns, P. Moerman, 1999, American journal of medical genetics.

P3-14-22: Response to Neoadjuvant Chemotherapy in Elderly Patients with Locally Advanced Breast Cancer.

P. Neven, R. Paridaens, M. Christiaens, 2011 .

Transition of endometrial stromal sarcoma into high-grade sarcoma.

P. Neven, I. Vergote, F. Amant, 2006, Gynecologic oncology.

Dormant foci of endometrial stromal sarcoma as an intermediate between an indolent and aggressive growth

F. Amant, P. Moerman, I. Vergote, 2007 .

Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her child.

J. Fryns, P. Moerman, 1996, American journal of medical genetics.

Trisomy 21 in a second trimester male hydropic fetus with "Noonan-syndrome-phenotype": nuchal and thoracic lymphangiomatosis, oedema of the dorsum of hands and feet, and bicuspid pulmonary valve.

J. Fryns, P. Moerman, 1998, Genetic counseling.

Peritoneal "pearl" mystery after uterine artery embolization.

P. Moerman, W. Poppe, G. Maleux, 2011, Journal of vascular and interventional radiology : JVIR.

ELEVATED MATERNAL SERUM AND AMNIOTIC FLUID ALPHA‐FETOPROTEIN LEVELS IN THE DENYS–DRASH SYNDROME

K. Devriendt, J. Fryns, P. Moerman, 1996, Prenatal diagnosis.

Wilms' Tumor Gene 1 (wt1) Overexpression in Neurons in Deep Endometriosis: a Pilot Study Article in Press

F. Amant, A. Coosemans, P. Moerman, 2022 .

Apparently new "anophthalmia-plus" syndrome in sibs.

J. Fryns, E. Legius, P. Moerman, 1995, American journal of medical genetics.

NEWS ON ULTRASONOGRAPHIC TECHNIQUES FOR PELVIC MALIGNANCIES

B. De Moor, D. Timmerman, S. Van Huffel, 2003, International Journal of Gynecologic Cancer.

Four cytogenetic subgroups can be identified in endometrial polyps.

P. D. Dal Cin, P. Cin, W. V. D. Van de Ven, 1995, Cancer research.

Who needs adjuvant systemic treatment ? Predicting prognosis in node-negative breast cancer ; from bench to bedside

P. Neven, V. Belle, M. Christiaens, 2009 .

Biology and prognosis by age of primary operable breast cancer.

Patrick Neven, S. Van Huffel, Frédéric Amant, 2009 .

Breast cancer phenotype, nodal status and palpability may be useful in the detection of overdiagnosed screening-detected breast cancers.

E. van Limbergen, P. Neven, E. Kellen, 2013 .

Premature closure of the foramen ovale and congenital pulmonary cystic lymphangiectasis in aortic valve atresia or in severe aortic valve stenosis.

P. Moerman, H. van Dijck, L. Van der hauwaert, 1986, The American journal of cardiology.

Wilms' tumor gene 1 (WT1) overexpression in neurons in deep endometriosis: a pilot study.

F. Amant, A. Coosemans, P. Moerman, 2009, Fertility and sterility.

Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes

T. Mazza, H. Van Esch, H. Kayserili, 2016, Journal of Medical Genetics.

Holoprosencephaly and postaxial polydactyly: another observation.

J. Fryns, P. Moerman, 1988, Journal of medical genetics.

Clinical study investigating the role of lymphadenectomy, surgical castration and adjuvant hormonal treatment in endometrial stromal sarcoma

P. Neven, F. Amant, B. Calster, 2007, British Journal of Cancer.

Normal testicular histology in a mid‐trimester 49,XXXXY fetus

P. Moerman, J. Fryns, A. Kleczkowska, 1995, Clinical genetics.

THE POSITIVE ASSOCIATION BETWEEN BREAST TUMOR SIZE AND LYMPH NODE INVOLVEMENT IN LOBULAR BREAST CANCERS IS PROGESTERONE RECEPTOR DEPENDENT

P. Neven, R. Paridaens, H. Wildiers, 2010 .

Polyhydramnios as a prenatal symptom of the DiGeorge/velo‐cardio‐facial syndrome

K. Devriendt, B. Eyskens, J. Fryns, 1998, Prenatal diagnosis.

Fetal Caudal Dysgenesis after Maternal Cardiopulmonary Bypass in Pregnancy

F. Rademakers, J. Fryns, P. Moerman, 2007 .