A. Bröcker-Vriends

发表

Mortality and causes of death in Dutch haemophiliacs, 1973–86

J. Vandenbroucke, F. Rosendaal, J. Hermans, 1989, British journal of haematology.

Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study

J. Klijn, H. Meijers-Heijboer, C. Seynaeve, 2006, Clinical genetics.

Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)

E. Kuipers, J. Houwing-Duistermaat, T. Reinards, 2005, Journal of Medical Genetics.

Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).

A. Wagner, H. Morreau, M. Breuning, 2006, Gastroenterology.

The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B

P. Reitsma, G. Ommen, E. Bakker, 2005, Annals of Hematology.

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

A. Zwinderman, R. Hofstra, A. Wagner, 2001, Journal of medical genetics.

The common sense model of self‐regulation and psychological adjustment to predictive genetic testing: a prospective study

J. Klijn, H. Meijers-Heijboer, C. Seynaeve, 2007, Psycho-oncology.

Bannayan–Riley–Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases

L. Hoefsloot, M. Breuning, S. Kant, 2004, Familial Cancer.

The use of preventive health care services: carrier testing for the genetic disorder haemophilia.

F. Rosendaal, T. Suurmeijer, I. Varekamp, 1993, Social science & medicine.

Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene

P. Devilee, P. Taschner, C. Cornelisse, 2001, Genes, chromosomes & cancer.

Bleeding in carriers of hemophilia.

F. Rosendaal, H. K. V. van Amstel, J. G. van der Bom, 2006, Blood.

Prognostic factors for hereditary cancer distress six months after BRCA1/2 or HNPCC genetic susceptibility testing.

J. Klijn, H. Meijers-Heijboer, C. Seynaeve, 2007, European journal of cancer.

Experience of parental cancer in childhood is a risk factor for psychological distress during genetic cancer susceptibility testing.

J. Klijn, H. Meijers-Heijboer, C. Seynaeve, 2006, Annals of oncology : official journal of the European Society for Medical Oncology.

AIDS and haemophilia. A study among Dutch haemophiliacs on the psychological impact of the AIDS threat, the prevalence of HIV antibodies and the adoption of measures to prevent HIV transmission.

F. Rosendaal, T. Suurmeijer, I. Varekamp, 1988, Haemostasis.

Carrier testing and prenatal diagnosis for hemophilia: experiences and attitudes of 549 potential and obligate carriers.

F. Rosendaal, T. Suurmeijer, I. Varekamp, 1990, American journal of medical genetics.

Employment of individuals with haemophilia in The Netherlands.

F. Rosendaal, T. Suurmeijer, I. Varekamp, 1989, Social science & medicine.

Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis.

J. C. Houwelingen, F. Rosendaal, G. V. Ommen, 1991, Journal of medical genetics.

Comparison of individuals opting for BRCA1/2 or HNPCC genetic susceptibility testing with regard to coping, illness perceptions, illness experiences, family system characteristics and hereditary cancer distress.

J. Klijn, H. Meijers-Heijboer, C. Seynaeve, 2007, Patient education and counseling.

Physical condition, longevity, and social performance of Dutch haemophiliacs, 1972-85.

F. Rosendaal, T. Suurmeijer, I. Varekamp, 1989, BMJ.

Sex ratio of the mutation frequencies in haemophilia A: estimation and meta-analysis

J. C. Houwelingen, J. Vandenbroucke, F. Rosendaal, 1990, Human Genetics.

First trimester prenatal diagnosis of haemophilia A: Two years' experience

P. Pearson, J. Dreesen, H. Kanhai, 1988, Prenatal diagnosis.

Hemophilia and the use of genetic counseling and carrier testing within family networks.

F. Rosendaal, T. Suurmeijer, I. Varekamp, 1992, Birth defects original article series.

A near false‐negative finding of mosaic trisomy 21—a cautionary tale

F. Klumper, J. Roosmalen, G. Beverstock, 1998, Prenatal diagnosis.

Familial endometrial cancer in female carriers of MSH6 germline mutations

P. Møller, H. Meijers-Heijboer, R. Hofstra, 1999, Nature Genetics.

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance.

P. Møller, H. V. van Houwelingen, G. Kenter, 2004, Gastroenterology.

Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer

H. Meijers-Heijboer, A. Wagner, H. Morreau, 2004, Clinical Cancer Research.

Conventional and tissue microarray immunohistochemical expression analysis of mismatch repair in hereditary colorectal tumors.

H. Morreau, R. Fodde, P. Franken, 2003, The American journal of pathology.

Diagnostic Approach and Management of Lynch Syndrome (Hereditary Nonpolyposis Colorectal Carcinoma): A Guide for Clinicians

H. Morreau, M. Breuning, H. Vasen, 2006, CA: a cancer journal for clinicians.

Chapter 3 . 1 Bleeding in carriers of hemophilia

J. Bom, E. Mauser-Bunschoten, A. Bröcker-Vriends, 2005 .

Somatic origin of inherited haemophilia A

P. Reitsma, P. Pearson, J. Dreesen, 1990, Human Genetics.

Genotype Assignment of Haemophilia A by Use of Intragenic and Extragenic Restriction Fragment Length Polymorphisms

P. Pearson, J. Dreesen, R. Quadt, 1987, Thrombosis and Haemostasis.

lntragenic Restriction-Fragment Length Polymorphism

P. Pearson, R. Bertina, R. Quadt, 2018 .

A prospective study of the impact of genetic susceptibility testing for BRCA1/2 or HNPCC on family relationships

J. Klijn, H. Meijers-Heijboer, C. Seynaeve, 2007, Psycho-oncology.

Monosomy 8p: an easily overlooked syndrome.

G. Beverstock, A. Bröcker-Vriends, F. van Bel, 1986, Journal of medical genetics.

Bias in detection of instability of the (C)8 mononucleotide repeat of MSH6 in tumours from HNPCC patients

H. Morreau, C. Cornelisse, H. Vasen, 2001, Oncogene.

Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas.

P. Taschner, J. Romijn, M. Losekoot, 2005, European journal of endocrinology.

Unbalanced karyotype with normal phenotype in a family with translocation (8;13) (p21;q22)

J. Geraedts, A. Bröcker-Vriends, J. Kamp, 1985, Clinical genetics.

Identification of HNPCC by Molecular Analysis of Colorectal and Endometrial Tumors

H. Morreau, H. Vasen, A. Bröcker-Vriends, 2004, Disease markers.

Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.

A. Zwinderman, K. Heimdal, P. Møller, 1998, The New England journal of medicine.

Use of Gene Probes for Carrier Detection and Prenatal Diagnosis in Hemophilia A

A. Bröcker-Vriends, E. Briët, 1988 .