H. V. D. Berghe

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Trisomy 7 and trisomy 10 characterize subpopulations of tumor-infiltrating lymphocytes in kidney tumors and in the surrounding kidney tissue.

J. Delabie, P. Cin, L. Baert, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia.

P. Marynen, J. Grosgeorge, J. Cools, 1997, Blood.

Genomic instability and recurrent breakpoints are main cytogenetic findings in Hodgkin's disease.

B. Falini, C. Mecucci, M. Martelli, 1999, Haematologica.

Combined morphologic and karyotypic study of 28 myxoid liposarcomas. Implications for a revised morphologic typing, (a report from the CHAMP Group).

F. Mitelman, P. Cin, R. Sciot, 1996, The American journal of surgical pathology.

The apoptosis inhibitor gene API2 and a novel 18q gene, MLT, are recurrently rearranged in the t(11;18)(q21;q21) associated with mucosa-associated lymphoid tissue lymphomas.

P. Marynen, A. Hagemeijer, C. Wolf‐peeters, 1999, Blood.

Polyclonal primitive hematopoietic progenitors can be detected in mobilized peripheral blood from patients with high-risk myelodysplastic syndromes.

G. Verhoef, H. van den Berghe, P. Vandenberghe, 1995, Blood.

The Coffin‐Siris syndrome: Report of a family and further delineation

J. Fryns, H. Berghe, M. Haspeslagh, 1984, Clinical genetics.

Turner syndrome patients as adults: a study of their cognitive profile, psychosocial functioning and psychopathological findings.

J. Fryns, H. van den Berghe, A. Swillen, 1993, Genetic counseling.

"Small" B-cell non-Hodgkin's lymphomas with splenomegaly at presentation are either mantle cell lymphoma or marginal zone cell lymphoma. A study based on histology, cytology, immunohistochemistry, and cytogenetic analysis.

S. Pittaluga, C. Mecucci, C. de Wolf‐Peeters, 1996, The American journal of surgical pathology.

Mantle cell lymphoma: a clinicopathological study of 55 cases

S. Pittaluga, C. Wolf‐Peeters, C. Wolf‐peeters, 1995, Histopathology.

Iatrogenic multiple pregnancies in East Flanders, Belgium.

R. Vlietinck, C. Derom, H. Maes, 1993, Fertility and sterility.

The receptor-binding domain of human alpha 2-macroglobulin. Isolation after limited proteolysis with a bacterial proteinase.

P. Marynen, F. van Leuven, J. Cassiman, 1986, The Journal of biological chemistry.

Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features.

S. Pittaluga, C. Mecucci, C. Wolf‐peeters, 1996, Blood.

Cell surface heparan sulfate proteoglycans from human vascular endothelial cells. Core protein characterization and antithrombin III binding properties.

J. Cassiman, J. Cassiman, H. van den Berghe, 1992, The Journal of biological chemistry.

t(9;22)(q22-31;q11-12) is a consistent marker of extraskeletal myxoid chondrosarcoma: evaluation of three cases.

R. Sciot, C. Fletcher, R. Sciot, 1995, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells

D. Gisselsson, P. D. Dal Cin, M. Höglund, 1999, Human Genetics.

Molecular cloning of amphiglycan, a novel integral membrane heparan sulfate proteoglycan expressed by epithelial and fibroblastic cells

P. Marynen, J. Cassiman, H. van den Berghe, 1992, The Journal of cell biology.

Molecular delineation of 13q deletion boundaries in 20 patients with myeloid malignancies.

A. Aventín, C. Mecucci, M. Martelli, 1998, Blood.

Cutaneous sclerosing perineurioma with cryptic NF2 gene deletion.

A. Hagemeijer, P. Cin, R. Sciot, 1999, The American journal of surgical pathology.

Chronic myelogenous leukemia after treatment with 131I for thyroid carcinoma. Report of a case and review of the literature.

C. Mecucci, M. Stul, G. Verhoef, 1991, Cancer genetics and cytogenetics.

The IL-9 receptor gene, located in the Xq/Yq pseudoautosomal region, has an autosomal origin, escapes X inactivation and is expressed from the Y.

P. Marynen, J. Vermeesch, J. Renauld, 1997, Human molecular genetics.

Chromosome abnormalities in cementifying fibroma.

P. Cin, R. Sciot, R. Sciot, 1993, Cancer genetics and cytogenetics.

Four cytogenetic subgroups can be identified in endometrial polyps.

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

Cytogenetic analysis of subcutaneous angiolipoma: further evidence supporting its difference from ordinary pure lipomas: a report of the CHAMP Study Group.

F. Mitelman, P. Cin, R. Sciot, 1997, The American journal of surgical pathology.

Fertility in patients with X chromosome deletions

J. Fryns, A. Kleczkowska, H. V. D. Berghe, 1982, Clinical genetics.

The 6p21 chromosome region is nonrandomly involved in endometrial polyps.

P. Cin, H. van den Berghe, F. de Wolf, 1992, Gynecologic oncology.

Chromosome 11q rearrangements in B non Hodgkin's lymphoma

C. Mecucci, M. Stul, G. Verhoef, 1992, British journal of haematology.

Philadelphia chromosome-positive acute myeloid leukemia: cytoimmunologic and cytogenetic features.

P. Cin, M. Stul, A. Cuneo, 1996, Haematologica.

i(12p) in a malignant ovarian tumor.

F. Speleman, P. Cin, H. van den Berghe, 1990, Cancer genetics and cytogenetics.

Multiple distinct membrane heparan sulfate proteoglycans in human lung fibroblasts.

J. Cassiman, J. Cassiman, H. van den Berghe, 1989, The Journal of biological chemistry.

Fusion of ETV6 to MDS1/EVI1 as a result of t(3;12)(q26;p13) in myeloproliferative disorders.

P. Marynen, A. Hagemeijer, H. van den Berghe, 1997, Cancer research.

Clinical-cytogenetic correlations in myelodysplasia (preleukemia).

J. Rowley, O. Garson, F. Mitelman, 1989, Cancer genetics and cytogenetics.

The myelodysplastic syndromes: different evolution patterns based on sequential morphological and cytogenetic investigations

G. Tricot, C. Wolf‐Peeters, R. Verwilghen, 1985, British journal of haematology.

Osteoid osteoma and osteoblastoma with clonal chromosome changes.

R. Sciot, H. van den Berghe, P. Dal Cin, 1998, British Journal of Cancer.

Spatial and temporal changes in the expression of fibroglycan (syndecan-2) during mouse embryonic development.

P. Marynen, G. David, Xiao-mei Bai, 1993, Development.

Differential expression of cell surface heparan sulfate proteoglycans in human mammary epithelial cells and lung fibroblasts.

J. Cassiman, J. Cassiman, H. van den Berghe, 1992, The Journal of biological chemistry.

Localization of the gene (RSN) coding for restin, a marker for Reed-Sternberg cells in Hodgkin's disease, to human chromosome band 12q24.3 and YAC cloning of the locus.

J. Delabie, F. Speleman, F. van Leuven, 1994, Cytogenetics and cell genetics.

Inflammatory myofibroblastic tumor of bone: report of two cases with evidence of clonal chromosomal changes

P. Cin, R. Sciot, J. García, 1997 .

Aspects of the neoplasms observed in patients with constitutional autosomal trisomy.

H. van den Berghe, D. Satgé, H. V. D. Berghe, 1996, Cancer genetics and cytogenetics.

Translocation (X;1) reveals metastasis 31 years after renal cell carcinoma.

P. Cin, R. Sciot, R. Sciot, 1998, Cancer genetics and cytogenetics.

Partial primary structure of the 48- and 90-kilodalton core proteins of cell surface-associated heparan sulfate proteoglycans of lung fibroblasts. Prediction of an integral membrane domain and evidence for multiple distinct core proteins at the cell surface of human lung fibroblasts.

P. Marynen, J. Cassiman, J. Cassiman, 1989, The Journal of biological chemistry.

Cytogenetic and clinical investigations in 76 cases with therapy-related leukemia and myelodysplastic syndrome.

C. Mecucci, H. van den Berghe, M. Boogaerts, 1989, Cancer genetics and cytogenetics.

Collagen metabolism and basement membrane formation in cultures of mouse mammary epithelial cells. Induction of 'assembly' on fibrillar type I collagen substrata.

H. van den Berghe, G. David, B. Nusgens, 1987, Experimental cell research.

Long-term survival in acute myelogenous leukemia: a second follow-up of the Fourth International Workshop on Chromosomes in Leukemia.

C. Bloomfield, O. Garson, R. Berger, 1994, Cancer genetics and cytogenetics.

Fluorescence in situ hybridization characterization of new translocations involving TEL (ETV6) in a wide spectrum of hematologic malignancies.

P. Marynen, A. Hagemeijer, C. Mecucci, 1998, Blood.

On two patients with and without the classical Wolf‐Hirschhorn syndrome (WHS) sharing the same chromosome 4p16.3 specific probe deletion: evidence of a contiguous gene deletion syndrome

J. Fryns, H. Berghe, J. Schmit, 1996, Clinical genetics.

Induction of sister-chromatid exchanges in cultured human cells by an organophosphorous insecticide: malathion.

H. van den Berghe, A. H. Nicholas, M. Vienne, 1979, Mutation research.

Isochromosome 12p in mediastinal germ cell tumor.

P. Cin, H. van den Berghe, P. Dal Cin, 1989, Cancer genetics and cytogenetics.

Adults with Williams‐Beuren syndrome: evaluation of the medical, psychological and behavioral aspects

J. Fryns, H. Berghe, M. Borghgraef, 1994, Clinical genetics.

Intelligence, behaviour and psychosocial development in Turner syndrome. A cross-sectional study of 50 pre-adolescent and adolescent girls (4-20 years).

J. Fryns, H. van den Berghe, G. Massa, 1993, Genetic counseling.

Philadelphia chromosome in human multiple myeloma.

R. Verwilghen, H. van den Berghe, J. Michaux, 1979, Journal of the National Cancer Institute.

Chromosome 1p abnormalities in B non Hodgkin's lymphoma.

P. Cin, C. Mecucci, C. Wolf‐peeters, 1991, Leukemia & lymphoma.

A monoclonal antibody to a neo-antigen on alpha 2-macroglobulin complexes inhibits receptor-mediated endocytosis.

P. Marynen, F. van Leuven, J. Cassiman, 1981, Journal of immunology.

Expression of mouse alpha-macroglobulins, lipoprotein receptor-related protein, LDL receptor, apolipoprotein E, and lipoprotein lipase in pregnancy.

F. Leuven, S. Torrekens, K. Lorent, 1995, Journal of lipid research.

A physical map of the region spanning the chromosome 12 translocation breakpoint in a mesothelioma with a t(X;12)(q22;p13).

J. Vermeesch, J. Aerssens, M. Litt, 1995, Cytogenetics and cell genetics.

Recurrent chromosome aberrations in fibrous dysplasia of the bone: a report of the CHAMP study group. CHromosomes And MorPhology.

P. D. Dal Cin, F. Mitelman, P. Cin, 2000, Cancer genetics and cytogenetics.

A novel gene, AF-1p, fused to HRX in t(1;11)(p32;q23), is not related to AF-4, AF-9 nor ENL.

R. Berger, C. Mecucci, H. van den Berghe, 1994, Oncogene.

Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome?

J. Fryns, E. Legius, H. van den Berghe, 1989, Journal of medical genetics.

Monosomy 22 and trisomy 14 may be early events in the tumorigenesis of adult granulosa cell tumor.

P. Cin, H. van den Berghe, P. Dal Cin, 1999, Cancer genetics and cytogenetics.

Cytogenetic studies of 103 patients with acute myelogenous leukemia in relapse.

A. de la Chapelle, O. Garson, A. Hagemeijer, 1989, Cancer genetics and cytogenetics.

Philadelphia chromosome-positive chronic myelogenous leukemia in treated Hodgkin's disease.

C. Mecucci, M. Stul, J. Cassiman, 1990, Cancer genetics and cytogenetics.

Molecular characterization of the murinoglobulins.

F. van Leuven, F. Leuven, L. Overbergh, 1991, The Journal of biological chemistry.

Tertiary partial 14 trisomy 47, XX, +14q-

J. Fryns, J. Cassiman, J. Cassiman, 2004, Humangenetik.

Solubilization and affinity purification of the alpha 2-macroglobulin receptor from human fibroblasts.

P. Marynen, F. van Leuven, J. Cassiman, 1984, The Journal of biological chemistry.

Acute nonlymphoblastic leukemia with bone marrow eosinophilia and structural anomaly of chromosome 16.

C. Mecucci, H. van den Berghe, J. Michaux, 1985, Cancer genetics and cytogenetics.

A child, homozygous for a stop codon in exon 11, shows milder cystic fibrosis symptoms than her heterozygous nephew

P. Marynen, J. Cassiman, H. Berghe, 1990, Journal of medical genetics.

Clinical significance of cytogenetic abnormalities in uterine myomas.

P. Cin, J. Deprest, H. van den Berghe, 1998, Fertility and sterility.

Cytogenetic profile of minimally differentiated (FAB M0) acute myeloid leukemia: correlation with clinicobiologic findings.

P. Cin, M. Stul, A. Cuneo, 1995, Blood.

Inflammatory myofibroblastic tumor with HMGIC rearrangement.

R. Sciot, J. Bullerdiek, H. van den Berghe, 1999, Cancer genetics and cytogenetics.

Immunohistochemical localization of human α2macroglobulin in connective tissue

J. Cassiman, H. Berghe, F. Leuven, 2004, Cell and Tissue Research.

Bloom's Syndrome: Possible Pitfalls in Clinical Diagnosis

J. Fryns, H. van den Berghe, R. Eeckels, 1984 .

Chromosome studies in patients with Philadelphia chromosome-positive chronic myeloid leukemia submitted to bone marrow transplantation--results of a European Cooperative Study.

G. Rosti, M. Boogaerts, W. Arcese, 1987, Cancer genetics and cytogenetics.

Differences in the distribution and nature of the interstitial telomeric (TTAGGG)n sequences in the chromosomes of the Giraffidae, okapai (Okapia johnstoni), and giraffe (Giraffa camelopardalis): evidence for ancestral telomeres at the okapi polymorphic rob(5;26) fusion site.

P. Marynen, J. Vermeesch, H. van den Berghe, 1996, Cytogenetics and cell genetics.

Reciprocal translocation t(6;9)(p21;q33): a new characteristic chromosome anomaly in myeloid leukemias.

H. van den Berghe, J. Michaux, A. Louwagie, 1983, Cancer genetics and cytogenetics.

Congenital scalp defect, distal limb reduction anomalies, right spastic hemiplegia and hypoplasia of the left arteria cerebri media: Further evidence that interruption of early embryonic blood supply may result in Adams‐Oliver (plus) syndrome

J. Fryns, E. Legius, H. Berghe, 1996, Clinical genetics.

Translocation t(11;21)(q24;q11.2) is a new nonrandomly occurring chromosome change in myelodysplastic syndromes.

C. Mecucci, H. van den Berghe, M. Boogaerts, 1988, Cancer genetics and cytogenetics.