H. Berghe

发表

Predictive and preimplantation genetic testing for Huntington's disease and other late onset dominant disorders: not in conflict but complementary

K. Demyttenaere, R. Dom, J. Fryns, 1996, Clinical genetics.

Primary amines inhibit recycling of α 2M receptors in fibroblasts

J. Cassiman, H. Berghe, F. Leuven, 1980, Cell.

HMGI-C and HMGI(Y) Immunoreactivity Correlates with Cytogenetic Abnormalities in Lipomas, Pulmonary Chondroid Hamartomas, Endometrial Polyps, and Uterine Leiomyomas and is Compatible with Rearrangement of the HMGI-C and HMGI(Y) Genes

P. Cin, P. Pauwels, J. Bullerdiek, 2000, Laboratory Investigation.

The motivation of at‐risk individuals and their partners in deciding for or against predictive testing for Huntington's disease

J. Cassiman, G. Evers‐Kiebooms, H. Berghe, 1989, Clinical genetics.

A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy

J. Steyaert, J. Fryns, E. Legius, 1997, Clinical genetics.

Philadelphia‐positive acute myelomonocytic leukemia with inversion of chromosome 16 and eosinobasophils

C. Mecucci, H. Berghe, N. Testoni, 1988, American journal of hematology.

Bibliometric indicators of university research performance in Flanders

Henk F. Moed, Herman Van den Berghe, Renger E. de Bruin, 1998 .

A genetic‐diagnostic survey in an institutionalized population of 173 severely mentally retarded patients

J. Fryns, H. Berghe, A. Kleczkowska, 1986, Clinical genetics.

Cohen syndrome: fertility in a female patient

J. Fryns, H. Berghe, F. Lemmens, 1991, Clinical genetics.

Cohen syndrome: the clinical symptoms and stigmata at a young age

K. Devriendt, J. Fryns, E. Legius, 1996 .

Adolescents’ Attitude towards Carrier Testing for Cystic Fibrosis and Its Relative Stability over Time

G. Evers‐Kiebooms, M. Decruyenaere, H. Berghe, 1996, European journal of human genetics : EJHG.

Fibronectin-Mediated Cellular (Inter)Actions

B. Strooper, J. Cassiman, H. Berghe, 1989 .

Cytogenetics of tumours of the female reproductive tract

P. Cin, H. Berghe, 1994 .

ILX Lightwave, "LDT-5100 Application Notes", Bozeman, MT, 1997.

R. D. Irwin, Anil K. Jain, M. Altschuler, 1998 .

Alveolar soft‐part sarcoma: evidence for its myogenic origin and for the involvement of 17q25

V. Desmet, P. Cin, R. Sciot, 1993, Histopathology.

Genetic control over fragile X chromosome expression

F. Hecht, J. Fryns, R. Vlietinck, 1986, Clinical genetics.

Bibliometric Indicators of University Research Performance in Flanders

R. D. Bruin, H. Moed, H. Berghe, 1998, J. Am. Soc. Inf. Sci..

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

H. Berghe, F. Leuven, S. Torrekens, 1995 .

Human elongation factor 1α: a polymorphic and conserved multigene family with multiple chromosomal localizations

G. Volckaert, G. Opdenakker, A. Billiau, 1987, Human Genetics.

PRENATAL DIAGNOSIS OF HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLÆMIA Expression of a Genetic Receptor Disease in Utero

J. Fryns, P. Kovanen, J. Goldstein, 1978, The Lancet.

The 5q- syndrome.

H. Berghe, 2009 .

A new lethal syndrome with cloudy corneae, diaphragmatic defects and distal limb deformities

J. Fryns, H. Berghe, P. Goddeeris, 2004, Human Genetics.

Assignment of mouse α-2-macroglobulin gene to Chromosome 6 band F1-G3

H. Berghe, F. Leuven, L. Overbergh, 2004, Mammalian Genome.

Abstracts of workshop presentations (Part 6 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Qualitative and quantitative study of the growth and cell surface properties of Huntington's disease fibroblasts and age-matched controls

R. Vlietinck, J. Bellemans, J. Cassiman, 1979, Human Genetics.

The Floating‐Harbor syndrome: two affected siblings in a family

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

A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X‐linked mental retardation

J. Fryns, H. Berghe, M. Holvoet, 1991, Clinical genetics.

A genetic‐diagnostic survey in an institutionalized population of 158 mentally retarded patients. The Viaene experience

J. Fryns, H. Berghe, A. Dereymaeker, 1988, Clinical genetics.

Bibliometric Indicators of University Research Performance in Flanders

Henk F. Moed, Marc Luwel, Eric H. J. Spruyt, 1998, J. Am. Soc. Inf. Sci..

Mapping of human fibronectin receptorβ subunit gene to chromosome 10

B. Strooper, J. Cassiman, H. Berghe, 1988, Somatic cell and molecular genetics.

Detection of residual BCR/ABL transcripts in chronic myeloid leukaemia patients in complete remission using the polymerase chain reaction and nested primers

P. Martiat, J. Cassiman, H. Berghe, 1990, British journal of haematology.

Distinct haematological disorder with deletion of long arm of No. 5 chromosome

J. Fryns, J. Cassiman, H. Berghe, 1974, Nature.

An identical translocation between chromosome 1 and 15 in two patients with myelodysplastic syndromes

G. Tricot, C. Mecucci, H. Berghe, 1986, British journal of haematology.

Growth properties and in vitro life span of Alzheimer disease and Down syndrome fibroblasts. A blind study

R. Dom, J. Fryns, G. Carmeliet, 1990, Mechanisms of Ageing and Development.

The Wiedemann-Rautenstrauch or neonatal progeroid syndrome

H. Berghe, J. Leroy, J. Frijns, 1981, European Journal of Pediatrics.

Viral Hepatitis Type B: Studies of Congenital Transmission

H. Berghe, W. Liu, J. Desmyter, 2008 .

Cytogenetic, Clinical, and Morphologic Correlations in 78 Cases of Fibromatosis: A Report from the CHAMP Study Group

F. Mitelman, P. Cin, R. Sciot, 2000, Modern Pathology.

A cluster of α2-macroglobulin-related genes (α2M) on human chromosome 12p: cloning of the pregnancy-zone protein gene and an α2M pseudogene

P. Marynen, K. Devriendt, J. Cassiman, 1989 .

Chromosome 11q rearrangements in B non Hodgkin's lymphoma

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

Morphologic, immunologic and cytogenetic studies in erythroleukaemia: evidence for multilineage involvement and identification of two distinct cytogenetic‐clihicopathological types

P. Cin, A. Cuneo, G. Castoldi, 1990, British journal of haematology.

Deletions of the long arm of chromosome 7 in myeloid disorders: loss of band 7q32 implies worst prognosis

C. Mecucci, J. Dierlamm, Jesús M. Hernández, 1996, British journal of haematology.

T‐cell lymphoma developing in Hodgkin's disease: Evidence for two clones

J. Delabie, C. Mecucci, C. de Wolf‐Peeters, 1993, The Journal of pathology.

Mantle cell lymphoma: a clinicopathological study of 55 cases

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

Abstracts of workshop presentations (Part 2 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

No chromosome arm unturned: in memory of Roland Berger 1934–2012

A. Hagemeijer, O. Bernard, H. Berghe, 2014, Leukemia.

α2-Macroglobulin and other proteinase inhibitors do not interfere with the secretion of amyloid precursor protein in mouse neuroblastoma cells

B. Strooper, H. Berghe, F. Leuven, 1992 .

The amyloid beta protein precursor or proteinase nexin II from mouse is closer related to its human homolog than previously reported.

B. Strooper, H. Berghe, F. Leuven, 1991 .

Identification, molecular cloning, and characterization of the chromosome 12 breakpoint cluster region of uterine leiomyomas

J. Bullerdiek, E. Schoenmakers, J. Geurts, 1994, Genes, chromosomes & cancer.

chromosome A new hematologic syndrome with a distinct karyotype: the 5 q--

H. Berghe, M. Moriau, A. Cordier, 2011 .

Abstracts of workshop presentations (Part 12 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

The hand‐foot‐genital syndrome: on the variable expression in affected males

J. Fryns, H. Berghe, A. Vogels, 1993, Clinical genetics.

On the variable effect of mosaic normal/balanced chromosomal rearrangements in man

H. Berghe, J. Fryns, A. Kleczkowska, 1990, Journal of medical genetics.

The CF carrier status is not associated with a diminished self‐concept or increased anxiety: results of psychometric testing after at least 1 year

G. Evers‐Kiebooms, J. Cassiman, H. Berghe, 1996, Clinical genetics.

Cystic fibrosis: community knowledge and attitudes towards carrier screening and prenatal diagnosis

H. Berghe, Marlean Decruyenaere, Gerry Evers‐Klebooms, 1992, Clinical genetics.

Some genetic aspects of ovarian tumors

P. Cin, H. Berghe, 1998 .

Isochromosome (12p) in germ cell tumors.

P. Cin, H. Berghe, 1991 .

Aggregation-induced alterations in fibroblast morphology

J. Cassiman, H. Berghe, B. Schueren, 1976, Cell and Tissue Research.

A child with cystic fibrosis: I. Parental knowledge about the genetic transmission of CF and about DNA‐diagnostic procedures

G. Evers‐Kiebooms, H. Berghe, L. Denayer, 1990, Clinical genetics.

Cytogenetic-Morphologic Correlations in Aneurysmal Bone Cyst, Giant Cell Tumor of Bone and Combined Lesions. A Report from the CHAMP Study Group

F. Mitelman, P. Cin, R. Sciot, 2000, Modern Pathology.

The preservation and regeneration of cilia on human nasal epithelial cells cultured in vitro

J. Cassiman, J. Cassiman, H. Berghe, 2004, Archives of oto-rhino-laryngology.

Differential splicing of COL4A5 mRNA in kidney and white blood cells: A complex mutation in the COL4A5 gene of an alport patient deletes the NC1 domain

P. Marynen, J. Cassiman, H. Berghe, 1994, Pediatric Nephrology.

Differential splicing of COL4A5 mRNA in kidney and white blood cells: a complex mutation in the COL4A5 gene of an Alport patient deletes the NC1 domain.

P. Marynen, J. Cassiman, H. Berghe, 1993 .

Myeloid Malignancies Molecular Delineation of 13q Deletion Boundaries in 20 Patients With

A. Aventín, H. Berghe, R. L. Starza, 2011 .

VARIANT (3:21) TRANSLOCATION AND MEGAKARYOCYTIC INVOLVEMENT IN BLASTIC CRISIS OF PHILADELPHIA POSITIVE CHRONIC MYELOID LEUKAEMIA

A. Aventín, A. Delannoy, C. Mecucci, 1989, British journal of haematology.

HMG1 is not rearranged by 13q12 aberrations in lipomas

J. Bullerdiek, H. Berghe, P. Dal Cin, 1999, Genes, chromosomes & cancer.

Molecular characterization of mar, a multiple aberration region on human chromosome segment 12q13‐q15 implicated in various solid tumors

J. Bullerdiek, E. Schoenmakers, J. Geurts, 1995, Genes, chromosomes & cancer.

Analysis of Solid Tumours with Recurrent Breakpoints in Chromosome Region 12q13–15 by Fluorescence In Situ Hybridization Using a Microclone Library

J. Bullerdiek, E. Schoenmakers, B. Horsthemke, 1994 .

Development and Characterization of Cell Lines from a Myxoid Liposarcoma with t(12;16)(q13;p11.2) and Trisomy 8

P. Cin, J. Bullerdiek, H. Berghe, 1994 .

dup(12)(q13→qter) in two t(14;18)‐negative follicular b‐non‐hodgkin's lymphomas

P. Marynen, C. Mecucci, C. de Wolf‐Peeters, 1992, Genes, chromosomes & cancer.

SEGREGATION OF HLA B7 IN JUVENILE-ONSET DIABETES MELLITUS

R. Vlietinck, H. Berghe, C. Vermylen, 1976, The Lancet.

Variant translocation in Burkitt lymphoma

H. Berghe, G. Sokal, G. Cornu, 1979 .

THE PH1-CHROMOSOME: TRANSLOCATION TO CHROMOSOME 9

H. Berghe, 1973 .

Simultaneous occurrence of 5q− and 21q− in refractory anemia with thrombocytosis

R. Verwilghen, H. Berghe, H. van den Berghe, 1979 .

Rearrangements of immunoglobulin and TCR genes in lymphoid blast crisis of Ph + chronic myeloid leukaemia

P. Cin, C. Mecucci, M. Stul, 1990 .

Abstracts of workshop presentations (Part 10 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Transformation of polycythemia vera to myelofibrosis and late appearance of a 5q— Chromosome anomaly☆

R. Verwilghen, H. Berghe, J. Michaux, 1979 .

The Brachmann‐de Lange syndrome in two siblings of normal parents

J. Fryns, H. Berghe, G. Mertens, 1987, Clinical genetics.

CONGENITAL BOWING OF THE LONG BONES

J. Fryns, H. Berghe, P. Annicq, 1983, Acta paediatrica Scandinavica.

Adolescents' opinions about genetic risk information, prenatal diagnosis, and pregnancy termination

G. Evers‐Kiebooms, M. Decruyenaere, H. Berghe, 1995, Journal of medical genetics.

Dominant branchial cleft syndrome with characteristics of both branchio‐oto‐renal and branchio‐oculo‐facial syndrome

J. Fryns, E. Legius, H. Berghe, 1990, Clinical genetics.

De novo 3q/7q translocation and associated interstitial 7q35 deletion

J. Fryns, H. Berghe, A. Kleczkowska, 1988, Clinical genetics.

Primary mesodermal dysgenesis of the cornea (Peters' anomaly) in two brothers

J. Timmermans, J. Fryns, H. Berghe, 1979, Human Genetics.

Corneal clouding, subvalvular aortic stenosis, and midfacial hypoplasia associated with mental deficiency and growth retardation—A new syndrome?

J. Fryns, H. Berghe, 1979, European Journal of Pediatrics.

Oculocerebral syndrome with hypopigmentation (Cross syndrome): Report of two siblings born to consanguineous parents

G. Turner, J. Fryns, H. Berghe, 1988, Clinical genetics.

Gonadoblastoma and Y‐chromosome fluorescence

J. Fryns, H. Berghe, T. Lukusa, 1986 .

Unusual in vivo rearrangements of the Y‐chromosome in two males

J. Fryns, H. Berghe, A. Kleczkowska, 1987, Clinical genetics.

Unusual in vivo rearrangements of the Y chromosome with mitotic instability in vitro

J. Fryns, J. Cassiman, H. Berghe, 1978, Human Genetics.

Y to X translocation in man

J. Fryns, H. Berghe, P. Petit, 1977, Human Genetics.

An autosome-Y translocation restudied

J. Fryns, H. Berghe, G. David, 1973, Humangenetik.

Cytogenetic survey in couples with recurrent fetal wastage

H. Berghe, J. Fryns, A. Kleczkowska, 2004, Human Genetics.

Triploid-diploid mosaicism in the lymphocytes of a liveborn child with multiple malformations

H. Berghe, H. Verresen, 2004, Humangenetik.

The 4p- syndrome, with a report of two new cases

J. Fryns, H. Berghe, E. Eggermont, 2004, Humangenetik.

Myelodysplastic syndromes with bone marrow fibrosis: a myelodysplastic disorder with proliferative features

C. Wolf‐peeters, M. Stul, S. Deprez, 1991, Annals of Hematology.

Chromosomes in leukemia

A. Chapelle, F. Mitelman, J. Lindsten, 1977 .

presumably induced by benzene Chromosome analysis in two unusual malignant blood disorders

R. Verwilghen, H. Berghe, A. Louwagie, 2011 .

Chromosome analysis in two unusual malignant blood disorders presumably induced by benzene

R. Verwilghen, H. Berghe, A. Louwagie, 1979 .

Prenatal diagnosis of campomelic dwarfism

J. Fryns, H. Berghe, A. Assche, 1981, Clinical genetics.

On the familial occurrence of congenital bilateral absence of vas deferens

H. Berghe, J. Fryns, A. Kleczkowska, 1989, Clinical genetics.

Partial trisomy 14q due to familial t(14q-, 11q+) translocation

J. Fryns, H. Berghe, M. Eygen, 1977, Human Genetics.

Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours

Herman Van den Berghe, Jörn Bullerdiek, J. Bullerdiek, 1995, Nature Genetics.

Ten years of the cytogenetics of soft tissue tumors

P. Cin, H. Berghe, 1997 .

Mitochondrial DNA analysis on remains of a putative son of Louis XVI, King of France and Marie-Antoinette

R. Decorte, J. Moisan, A. Gilissen, 1998, European Journal of Human Genetics.

Klinefelter syndrome and two fragile X chromosomes

H. Berghe, J. Fryns, A. Kleczkowska, 1984, Clinical genetics.

Proximal duplication of the long arm of chromosome 10 (10q11.2 → 10q22): a distinct clinical entity

H. Berghe, J. Fryns, A. Kleczkowska, 1987, Clinical genetics.

Replication and inactivation of and isodicentric X: presence of an inactive centromere influences the replication patterns

J. Fryns, H. Berghe, P. Petit, 1983, Clinical genetics.

X‐chromosomes attached by their long arm: case report and replication kinetics of the rearranged X‐chromosome

J. Fryns, H. Berghe, P. Petit, 1982, Clinical genetics.

SCE variability in lymphocytes and fibroblasts

J. Cassiman, J. Cassiman, H. Berghe, 1988, Human Genetics.

The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25

Alfons Meindl, Marc Ladanyi, Takafumi Ueda, 2001, Oncogene.

Coffin-Lowry Syndrome

J. Fryns, H. Berghe, E. Moens, 2010 .

The Coffin syndrome

J. Fryns, H. Berghe, L. Vinken, 1977, Human Genetics.

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.

Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1

J. Fryns, H. Berghe, A. Kleczkowska, 1986, Clinical genetics.

Cytogenetic Findings in Moderate and Severe Mental Retardation A Study of an Institutionalized Population of 1991 Patients

H. Berghe, J. Fryns, A. Kleczkowska, 1984, Acta paediatrica Scandinavica. Supplement.

Eighth International Workshop on Human Gene Mapping

K. O. Elliston, D. Cox, K. Kidd, 1984 .

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.

Unusually long survival in a case of full triploidy of maternal origin

J. Fryns, H. Berghe, P. Goddeeris, 1977, Human Genetics.

Fluorescence in situ hybridization for the detection and monitoring of the Ph-positive clone in chronic myelogenous leukemia: comparison with metaphase banding analysis

A. Hagemeijer, A. Cuneo, M. Roberti, 1998, Leukemia.

Minor myeloid component in Ph chromosome‐positive acute lymphoblastic leukaemia: correlation with cytogenetic pattern and implication for poor response to therapy

M. Negrini, P. Cin, M. Stul, 1994, British journal of haematology.

Chromosomal abnormalities and their clinical significance in acute lymphoblastic leukemia. Third International Workshop on Chromosomes in Leukemia.

C. Bloomfield, J. Rowley, J. Whang‐Peng, 1983, Cancer research.

Tenth International Workshop on Human Gene Mapping

K. O. Elliston, D. Cox, K. Kidd, 1988 .

Trisomy 12 is uncommon in typical chronic lymphocytic leukaemias

C. Mecucci, M. Stul, H. Berghe, 1994, British journal of haematology.

Non‐radioactive in situ hybridization for the detection and monitoring of trisomy 12 in B‐cell chronic lymphocytic leukaemia

A. Cuneo, N. Piva, G. Castoldi, 1992, British journal of haematology.

Chromosome Abnormalities in Cutaneous B-Cell Lymphomas

C. Mecucci, M. Stul, J. Cassiman, 1994 .

Clinical implications of monosomy 7 in acute nonlymphocytic leukemia

A. Chapelle, J. Rowley, F. Mitelman, 1980 .

5q-Acute myelogenous leukemia [letter]

R. Verwilghen, H. Berghe, J. Michaux, 1976 .

Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission karyotype: 46,XX,-13,+t(13;13)(p11;q11)/46,XX,del(13)(p11)

J. Fryns, H. Berghe, P. Casaer, 1979, Human Genetics.

Excess of mental retardation and/or congenital malformation in reciprocal translocations in man

J. Fryns, H. Berghe, A. Kleczkowska, 2004, Human Genetics.

The Greig polysyndactyly craniofacial dysmorphism syndrome: Variable expression in a family

J. Fryns, H. Berghe, G. V. Noyen, 1981, European Journal of Pediatrics.

The Greig polysyndactyly-craniofacial dysmorphism syndrome

J. Fryns, H. Berghe, W. Coeck, 1977, European Journal of Pediatrics.

Short stature, craniofacial dysmorphism and dento‐skeletal abnormalities in a large kindred

J. Fryns, H. Berghe, E. Lebas, 1977, Clinical genetics.

Pericentric inversions in man: personal experience and review of the literature

J. Fryns, H. Berghe, J. Fryns, 2004, Human Genetics.

Paracentric inversion in man: Personal experience and review of the literature

J. Fryns, H. Berghe, 2004, Human Genetics.

Partial trisomy 1, karyotype 46,XY,12-,t(1q, 12p)+

J. Fryns, H. Berghe, M. Eygen, 1973, Humangenetik.

Chromosomes in plasma‐cell malignancies *

H. Berghe, 1989 .

Is t(6;20) (p21;q13) a characteristic chromosome change in endometrial polyp?

F. Speleman, P. Cin, H. Berghe, 1991 .

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

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

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.

A child with cystic fibrosis: II. Subsequent family planning decisions, reproduction and use of prenatal diagnosis

G. Evers‐Kiebooms, H. Berghe, L. Denayer, 1990, Clinical genetics.

The relative risk for standard 21 trisomy has not increased in young mothers in Belgium, 1960–1978

R. Vlietinck, G. Evers‐Kiebooms, H. Berghe, 1985, Clinical genetics.

Moderate mental-retardation and atypical phenotype in mosaic 18 trisomy

J. Fryns, H. Berghe, A. Lambrechts, 1979 .

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

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

Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotype

J. Fryns, H. Berghe, J. Marien, 1979, Human Genetics.

Partial trisomy 18q in a newborn with typical 18 trisomy phenotype

J. Fryns, H. Berghe, F. Detavernier, 1978, Human Genetics.

Population cytogenetics of autosomal fragile sites

F. Hecht, J. Fryns, H. Berghe, 1986, Clinical genetics.

“Spontaneous” FRA16B is a hot spot for sister chromatid exchanges

J. Fryns, J. Cassiman, H. Berghe, 1991, Human Genetics.

Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome

P. Marynen, K. Devriendt, J. Fryns, 1989, Human Genetics.

Mosaic tetrasomy 21 in severe mental handicap

J. Fryns, H. Berghe, J. Geutjens, 1982, European Journal of Pediatrics.

Partial trisomy 13: Karyotype 46,XY,-6,+t(13q,6q)

J. Fryns, H. Berghe, E. Eggermont, 1974, Humangenetik.

Malignant rhabdoid tumour of the liver. A case report

V. Desmet, P. Cin, H. Berghe, 1992, Histopathology.

Hydrometrocolpos—Polydactyly syndrome in a macerated female foetus

J. Fryns, H. Berghe, J. Lauweryns, 1981, European Journal of Pediatrics.

Partial monosomy of the long arm of chromosome 16 in a malformed newborn: Karyotype 46,XX,del(16)(q21)

J. Fryns, H. Berghe, J. Jaeken, 1977, Human Genetics.

Functional modifications of α2-macroglobulin by primary amines. Kinetics of inactivation of α2-macroglobulin by methylamine, and formation of anomalous complexes with trypsin

J. Cassiman, H. Berghe, F. Leuven, 1982 .

Immunohistochemical localization of human α2macroglobulin in connective tissue

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

MONOCLONAL ANTIBODIES TOWARD THE RECEPTOR‐RECOGNITION SITE ON α2‐MACROGLOBULIN COMPLEXES a

P. Marynen, J. Cassiman, H. Berghe, 1983 .

Isochromosome 17 q in Blast Crisis of Chronic Myeloid Leukemia and in Other Hematologic Malignancies Is the Result of Clustered Breakpoints in 17 p 11 and Is Not Associated With Coding TP 53 Mutations

Å. Borg, M. Höglund, B. Johansson, 1999 .

Trisomy 12p due to familial t(12p-,6q+) translocation

J. Fryns, J. Cassiman, H. Berghe, 2004, Humangenetik.

Partial trisomy 8: Trisomy of the distal part of the long arm of chromosome number 8+(8q2) in a severely retarded and malformed girl

J. Fryns, J. Cassiman, H. Berghe, 2004, Humangenetik.

Fragile (X) syndrome: a study of the psychological profile in 23 prepubertal patients

J. Fryns, H. Berghe, K. Pyck, 1987, Clinical genetics.

Malformative syndrome associated with a ring 10 chromosome and a translocated 10q/19 chromosome

J. Fryns, H. Berghe, J. Jaeken, 1978, Human Genetics.

Pleuropulmonary blastoma (pulmonary blastoma of childhood): genetic link with other embryonal malignancies?

V. Desmet, P. Cin, R. Sciot, 1994, Histopathology.

Association between XV2c/CS7/KM19/D9 haplotypes and the ΔF508 mutation A study of 57 Belgian families

P. Marynen, R. Decorte, J. Fryns, 1990, Human Genetics.

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

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

Isodicentric (X)(q13) in haematological malignancies: presentation of five new cases, application of fluorescence in situ hybridization (FISH) and review of the literature

C. Mecucci, J. Dierlamm, L. Michaux, 1995, British journal of haematology.

Interstitial deletion of the long arm of chromosome 2 in a polymalformed newborn-karyotype: 46,XX,del(2)(q21;q24)

J. Fryns, H. Berghe, H. Malbrain, 1977, Human Genetics.

Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiency

J. Fryns, H. Berghe, J. Jaeken, 2004, Human Genetics.

Partial 8p trisomy due to interstitial duplication: karyotype: 46, XX, inv dup(8) (p21.1→p22)

J. Fryns, H. Berghe, A. Kleczkowska, 1985, Clinical genetics.

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

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

Trisomy 3 is a consistent chromosome change in malignant lymphoproliferative disorders preceded by cold agglutinin disease

A. Delannoy, C. Mecucci, M. Stul, 1995, British journal of haematology.

The female and the fragile X syndrome: data on clinical and psychological findings in 7 fra(X) carriers

J. Fryns, H. Berghe, M. Borghgraef, 1990, Clinical genetics.

Congenital scalp defect with distal limb reduction anomalies

J. Fryns, H. Berghe, L. Corbeel, 1977, European Journal of Pediatrics.

Internal male pseudohermaphroditism in a 6 week old child

J. Fryns, H. Berghe, T. Lukusa, 1986, European Journal of Pediatrics.

Melkersson‐Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocation

J. Fryns, H. Berghe, E. Smeets, 1994, Clinical genetics.

Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization

S. Pittaluga, A. Hagemeijer, A. Raap, 1997, Leukemia.

Congenital scalp defects associated with postaxial polydactyly

J. Fryns, H. Berghe, 1979, Human Genetics.

Scalp defect associated with postaxial polydactyly: Confirmation of a distinct entity with autosomal dominant inheritance

J. Fryns, H. Berghe, P. Jonckheere, 2004, Human Genetics.

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.

Blastic phase of Ph1-positive chronic myeloid leukemia and t(3;21) [letter]

A. Aventín, C. Mecucci, H. Berghe, 1988 .

Morphologic, immunologic and cytogenetic (MIC) working classification of the acute myeloid leukaemias. Second MIC Cooperative Study Group.

H. Berghe, 1988, British journal of haematology.

Thrombocytosis and inv(3)(q21q26) [letter]

C. Mecucci, H. Berghe, 1983 .

The cryptic inv(2)(p23q35) defines a new molecular genetic subtype of ALK-positive ALCL

B. Falini, C. Wolf‐peeters, S. Morris, 1998 .

The marriage of pathology and genetics in soft tissue tumours: EACR--Mühlbock Memorial Lecture.

H. Berghe, 1996 .

Facial paralysis at the age of 2 months as a first clinical sign of van Buchem disease (endosteal hyperostosis)

J. Fryns, H. Berghe, 2004, European Journal of Pediatrics.

Alopecia‐mental retardation syndrome associated with convulsions and hypergonadotropic hypogonadism

K. Devriendt, J. Fryns, H. Berghe, 1996, Clinical genetics.

Cytogenetic characterization of congenital or infantile fibrosarcoma

H. Berghe, P. Brock, I. Wever, 1991, European Journal of Pediatrics.

Localization of a highly antigenic human fibroblast surface glycoprotein (FSG) on fibroblasts and on epithelia involved in secretion or resorption

J. Cassiman, H. Berghe, F. Leuven, 1981, Virchows Archiv. B, Cell pathology including molecular pathology.

Sex chromatin and cytogenetic survey of 10417 adult males and 357 children institutionalized in Belgian institutions for mentally retarded patients

J. Fryns, H. Berghe, J. D. Roover, 1975, Human Genetics.

9p trisomy/18p distal monosomy and multiple cutaneous leiomyomata

J. Fryns, H. Berghe, M. Haspeslagh, 1985, Human Genetics.

Partial duplication of the short arm of chromosome 9 (p13→p22) in a child with typical 9p trisomy phenotype

J. Fryns, H. Berghe, P. Casaer, 1979, Human Genetics.

Germinal mosaicism in achondroplasia: a family with 3 affected siblings of normal parents

J. Fryns, H. Berghe, A. Kleczkowska, 1983, Clinical genetics.

Mental retardation, craniofacial dysmorphism, hypogonadism, diabetes mellitus and epilepsy in four siblings. A “new” mental retardation syndrome

J. Fryns, H. Berghe, A. Vogels, 1990, Clinical genetics.

X‐chromosome polysomy in the female: personal experience and review of the literature

J. Fryns, H. Berghe, A. Kleczkowska, 1983, Clinical genetics.

Nuclear sexing in a population of Congolese metropolitan newborns.

H. Berghe, 1970 .

The psychological profile of the fragile X syndrome

H. Berghe, J. Fryns, J. Jacobs, 1984, Clinical genetics.

Trisomy-4 Identifies a Subset of Acute Nonlymphocytic Leukemias

G. Tricot, A. Delannoy, C. Mecucci, 1986 .

Deletion of the short arm of chromosome 9

J. Fryns, H. Berghe, G. Fabry, 1980, European Journal of Pediatrics.

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.

18q- syndrome in mother and daughter

J. Fryns, H. Berghe, M. Eygen, 1979, European Journal of Pediatrics.

Outward-rectifying chloride channels in cultured adult and fetal human nasal epithelial cells

J. Cassiman, H. Berghe, E. Carmeliet, 1990, The Journal of Membrane Biology.

A new chromosome anomaly in acute lymphoblastic leukemia (ALL)

R. Verwilghen, H. Berghe, E. Eggermont, 1979, Human Genetics.

Identification of a voltage- and calcium-dependent non-selective cation channel in cultured adult and fetal human nasal epithelial cells

J. Cassiman, H. Berghe, E. Carmeliet, 1990, Pflügers Archiv.

Molecular mapping of the chromosome 11 breakpoint of t(11;17)(q13;q21) in a t(11;14)(q13;q32)‐positive B non‐Hodgkin's lymphoma

W. V. D. Van de Ven, E. Schoenmakers, H. Berghe, 1993, Genes, chromosomes & cancer.

Multiple chromosomally distinct cell populations in myelodysplastic syndromes and their possible significance in the evolution of the disease

G. Tricot, C. Mecucci, H. Berghe, 1986, British journal of haematology.

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.

Ring chromosome 22 in a mentally retarded child and mosaic 45,XX,-15,-22,+t(15;22)(p11;q11)/ 46,XX,r(22)/46,XX karyotype in the mother

J. Fryns, H. Berghe, 1979, Human Genetics.

Malformative syndrome with ring chromosome 13

J. Fryns, J. Cassiman, H. Berghe, 2004, Humangenetik.

Full monosomy 21: A clinically recognizable syndrome?

J. Fryns, H. Berghe, P. Goddeeris, 1977, Human Genetics.

X/X translocation in a patient with Turner's syndrome

J. Fryns, H. Berghe, C. Soyez, 1973, Humangenetik.

Interstitial delection of the long arm of chromosome 8

J. Fryns, H. Berghe, M. Eygen, 2004, Human Genetics.

Ring chromosome 15 syndrome

J. Timmermans, J. Fryns, H. Berghe, 1979, Human Genetics.

Moderate mental retardation and nonspecific dysmorphic syndrome associated with ring chromosome 9

J. Fryns, H. Berghe, A. Lambrechts, 2004, Human Genetics.

Partial monosomy of the short arm of chromosome 9

J. Fryns, H. Berghe, J. Deroover, 1978, Human Genetics.

Partial duplication of the short arm of chromosome 10

J. Fryns, H. Berghe, J. Deroover, 1979, Human Genetics.

8q24.12 Interstitial deletion in trichorhinophalangeal syndrome type I

J. Fryns, H. Berghe, 1986, Human Genetics.

Langer-Giedion syndrome and deletion of the long arm of chromosome 8

J. Fryns, H. Berghe, M. Eygen, 2004, Human Genetics.

Langer-Giedion syndrome and deletion of the long arm of chromosome 8. Confirmation of the critical segment to 8q23

J. Fryns, H. Berghe, G. Heremans, 2004, Human Genetics.

Familial occurrence of severe ulnar aplasia and lobster claw feet: A new syndrome

J. Dequeker, J. Fryns, H. Berghe, 1978, Human Genetics.

Complex Chromosomal Rearrangement in a Mentally Retarded Boy without Gross Dysmorphic Stigmata

H. Berghe, J. Fryns, A. Kleczkowska, 1984, Acta paediatrica Scandinavica.

Abstracts of workshop presentations (Part 3 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Trisomy (18q) and tetrasomy (18p) resulting from isochromosome formation

J. Fryns, H. Berghe, A. Kleczkowska, 1986, Clinical genetics.

Deletion of 5q

M. L. Beau, A. Bernheim, H. Berghe, 1984 .

The probabilistic interpretation of correlation coefficients in population genetics

J. Cassiman, H. Berghe, E. Meulepas, 1991 .

Community attitudes towards prenatal testing for congenital handicap

G. Evers‐Kiebooms, M. Decruyenaere, H. Berghe, 1993 .

Second International Workshop on Chromosomes in Solid Tumors January 18–20, 1987: Conference summary

H. Berghe, 1987 .

Paracentric inversions in man

J. Fryns, H. Berghe, A. Kleczkowska, 1986, Human Genetics.

Two-dimensional shape decomposition using fuzzy subset theory applied to automated chromosome analysis

André Oosterlinck, H. Van den Berghe, L. Vanderheydt, 1981, Pattern Recognit..

Impact of genetic counseling: A review of published follow‐up studies

G. Evers‐Kiebooms, H. Berghe, 1979, Clinical genetics.

A stigmatizing effect of the carrier status for cystic fibrosis?

G. Evers‐Kiebooms, J. Cassiman, H. Berghe, 1994, Clinical genetics.

Female pseudohermaphroditism with complete masculinisation of the external genitalia in two siblings. A new entity?

J. Fryns, H. Berghe, K. Vandenberghe, 1984, European Journal of Pediatrics.

Nager type of Acrofacial dysostosis: an example of autosomal dominant transmission with variable expression

J. Fryns, K. Chrzanowska, H. Berghe, 1991 .

Calcification of cartilages, brachytelephalangy and peripheral pulmonary stenosis. Confirmation of the Keutel syndrome

J. Fryns, H. Berghe, P. Mattelaer, 1984, European Journal of Pediatrics.

De novo Robertsonian D/D type translocations: the Leuven experience

H. Berghe, J. Fryns, A. Kleczkowska, 1989, Clinical genetics.

Mental retardation with pterygia, shortness and distinct facial appearance A new MCA/MR syndrome

J. Fryns, H. Berghe, M. Haspeslagh, 1985, Clinical genetics.

Further evidence for the location of the blepharophimosis syndrome (BPES) at 3q22.3‐q23

J. Fryns, H. Berghe, P. Strømme, 1993, Clinical genetics.

Partial monosomy of the long arm of chromosome 16: A distinct clinical entity?

J. Fryns, H. Berghe, J. Bande-Knops, 1979, Human Genetics.

Tetraploidy with hydrops fetalis, cystic nuchal hygroma and 90, XX karyotype

J. Fryns, H. Berghe, K. Vandenberghe, 1987, Clinical genetics.

X-chromosome polysomy in the male

J. Fryns, H. Berghe, A. Kleczkowska, 1988, Human Genetics.

Chromosome Analysis of Leukemia and Preleukemia: Preliminary Data on the Possible Role of Environmental Agents

H. Berghe, 1984 .

On the nosology of the “primary true microcephaly, chorioretinal dysplasia, lymphoedema” association

J. Fryns, H. Berghe, E. Smeets, 1995, Clinical genetics.

Transmission of fragile (X)(q27) from normal male(s)

J. Fryns, H. Berghe, 1982, Human Genetics.

Psychological aspects of amniocentesis: anxiety feelings in three different risk groups

G. Evers‐Kiebooms, H. Berghe, A. Swerts, 1988, Clinical genetics.

Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patients

J. Fryns, K. Chrzanowska, H. Berghe, 1989, Clinical genetics.

The Dubowitz syndrome in a teenager

J. Fryns, H. Berghe, G. Fabry, 1979 .

Interstitial deletion of the short arm of chromosome 2 in a moderately mentally retarded boy without gross clinical stigmata

J. Fryns, H. Berghe, P. Waele, 1979, Human Genetics.

A peculiar subphenotype in the fra(X) syndrome: extreme obesity‐short stature‐stubby hands and feet‐diffuse hyperpigmentation. Further evidence of disturbed hypothalamic function in the fra(X) syndrome?

J. Fryns, H. Berghe, A. Dereymaeker, 1987, Clinical genetics.

Sex-linked recessive inheritance in Charcot-Marie-Tooth disease with partial clinical manifestations in female carriers

J. Fryns, H. Berghe, 2004, Human Genetics.

Inactivation pattern of the fragile X in heterozygous carriers

H. Berghe, J. Fryns, A. Kleczkowska, 1988, Human Genetics.

Non-infectious intracisternal A-type particles in a sarcoma-positive, leukemia-negative mouse cell line transformed by murine sarcoma virus (MSV)

A. Billiau, H. Berghe, H. Eyssen, 2005, Archiv für die gesamte Virusforschung.

Autosomal whole arm translocations in man

J. Fryns, H. Berghe, A. Kleczkowska, 1986, Clinical genetics.

Balanced transmission of centromeric fission products in man

J. Fryns, L. Hens, H. Berghe, 2004, Human Genetics.

INCREASED MONOZYGOTIC TWINNING RATE AFTER OVULATION INDUCTION

M. Thiéry, R. Vlietinck, C. Derom, 1987, The Lancet.

Zygosity determination in newborn twins using DNA variants.

M. Thiéry, P. Pearson, E. Bakker, 1985, Journal of medical genetics.

A new hematologic syndrome with a distinct karyotype: the 5 q--chromosome.

H. Berghe, H. van den Berghe, M. Moriau, 1975, Blood.

An improved procedure to quickly isolate and sequence the termini of DNA inserts of yeast artificial chromosomes

E. Schoenmakers, J. Geurts, H. Berghe, 1994 .

The 49,XXXXY syndrome. Clinical and psychological follow‐up data

J. Fryns, H. Berghe, E. Smeets, 1988, Clinical genetics.

Chromosome Abnormalities in Adenocarcinoma of the Prostate

P. Cin, H. Berghe, 1996 .

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

P. Marynen, X. Bai, J. Cassiman, 1993, Development.

Prenatal growth retardation, microphthalmos/iris coloboma, cloudy cornea, urogenital anomalies and microcephaly. A possible new sublethal syndrome

J. Fryns, H. Berghe, H. Verresen, 1997, Clinical genetics.

Cytogenetic and fluorescence in situ hybridization investigation of ring chromosomes characterizing a specific pathologic subgroup of adipose tissue tumors.

P. Cin, R. Sciot, W. V. D. Van de Ven, 1993, Cancer genetics and cytogenetics.

An apparently new autosomal recessive syndrome with facial dysmorphism, macrocephaly, myopia and Dandy‐Walker malformation

H. Berghe, J. Fryns, M. Buttiens, 1989 .

Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.

F. Mitelman, R. Sciot, W. V. D. Van de Ven, 1996, The American journal of pathology.

Correlation between clinicopathological features and karyotype in spindle cell sarcomas. A report of 130 cases from the CHAMP study group.

F. Mitelman, P. Cin, R. Sciot, 1999, The American journal of pathology.

Trisomy 3q11-q29 is recurrently observed in B-cell non-Hodgkin's lymphomas associated with cold agglutinin syndrome

A. Hagemeijer, J. Dierlamm, L. Michaux, 1998, Annals of Hematology.

The Aarskog syndrome

J. Fryns, H. Berghe, J. Macken, 1978, Human Genetics.

Cloning and molecular characterization of part of a new gene fused to HMGIC in mesenchymal tumors.

P. Cin, J. Bullerdiek, H. Berghe, 1998, The American journal of pathology.

Biallelic alterations of both ETV6 and CDKN1B genes in a t(12;21) childhood acute lymphoblastic leukemia case.

P. Marynen, C. Mecucci, J. Aerssens, 1996, Cancer research.

A new characteristic karyotypic anomaly in lymphoproliferative disorders

H. Berghe, H. van den Berghe, G. Sokal, 1979, Cancer.

Perception of predictive testing for Huntington's disease by young women: preferring uncertainty to certainty?

G. Evers‐Kiebooms, M. Decruyenaere, H. Berghe, 1993, Journal of medical genetics.

The clinical significance of karyotype in acute myelogenous leukemia.

C. Bloomfield, J. Rowley, A. de la Chapelle, 1989, Cancer genetics and cytogenetics.

Secondary chromosome changes in mantle cell lymphoma.

S. Pittaluga, A. Hagemeijer, H. Berghe, 1999, Haematologica.

Isolation of a somatic cell hybrid retaining the der(16)t(12;16)(q13;p11.2) from a myxoid liposarcoma cell line.

W. V. D. Van de Ven, J. Bullerdiek, H. Berghe, 1993, Cytogenetics and cell genetics.

“Adult” form of polycystic kidney disease in neonates

J. Fryns, H. Berghe, 1979, Clinical genetics.

Partial trisomy of the short arm of chromosome 3 (3p25→3pter)

J. Fryns, H. Berghe, C. Parloir, 2004, Human Genetics.

Partial trisomy for the long arm of chromosome 3 [3(q21→qter)+] in a newborn with minor physical stigmata

J. Fryns, H. Berghe, M. Eygen, 1978, Human Genetics.

A newborn with the cat-eye syndrome

J. Fryns, H. Berghe, E. Eggermont, 2004, Humangenetik.

Cytogenetic analysis of a mesenchymal hamartoma of the liver.

F. Speleman, P. Cin, H. Berghe, 1989, Cancer genetics and cytogenetics.

The t(1; 12)(p36;q13) in a Renal Oncocytoma

R. Sciot, L. Baert, H. V. Van Poppel, 1996, Genes, Chromosomes and Cancer.

On the variable effect of mosaic chromosomal rearrangements in man

H. Berghe, J. Fryns, A. Kleczkowska, 2022 .

Prediction of psychological functioning one year after the predictive test for Huntington's disease and impact of the test result on reproductive decision making.

K. Demyttenaere, R. Dom, J. Fryns, 1996, Journal of medical genetics.

Predictive testing for Huntington's disease: risk perception, reasons for testing and psychological profile of test applicants.

K. Demyttenaere, R. Dom, J. Fryns, 1995, Genetic counseling.

8/21 translocation in acute myeloid leukaemia.

G. Tricot, H. Berghe, H. van den Berghe, 2009, Scandinavian journal of haematology.

Interstitial 9q- deletions in hematologic malignancies.

G. Tricot, C. Mecucci, H. Berghe, 1984, Cancer genetics and cytogenetics.

The tetraphocomelia-cleft palate syndrome in identical twins

H. Berghe, P. Goddeeris, F. Moerman, 1980, Human Genetics.

Frontonasal malformation and reciprocal translocation t(15;22)(q22;q13)

J. Fryns, H. Berghe, A. Kleczkowska, 1993, Clinical genetics.

Lesions of 13q may occur independently of deletion of 16q in spindle cell/pleomorphic lipomas

R. Sciot, A. Cornelis, H. Berghe, 1997, Histopathology.

Family planning decisions after the birth of a cystic fibrosis child. The impact of prenatal diagnosis.

J. Cassiman, G. Evers‐Kiebooms, H. Berghe, 1988, Scandinavian journal of gastroenterology. Supplement.

Monosomy 22 in a malignant peripheral nerve sheath tumour of the kidney in childhood: a genetic link with other malignant paediatric renal neoplasms?

P. Cin, R. Sciot, C. Fletcher, 1995, Histopathology.

Partial trisomy 17q

J. Fryns, H. Berghe, C. Parloir, 1979, Human Genetics.

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.

Risk perception after CF carrier testing and impact of the test result on reproductive decision making.

G. Evers‐Kiebooms, J. Cassiman, H. Berghe, 1997, American journal of medical genetics.

Multiple Pterygium Syndrome type Escobar in two brothers Follow-up data from childhood to adulthood

J. Fryns, H. Berghe, P. Volcke, 1988, European Journal of Pediatrics.

Cytogenetic investigation of synchronous bilateral renal tumors.

P. Cin, L. Baert, H. V. Van Poppel, 1996, Cancer genetics and cytogenetics.

Congenital mesoblastic nephroma and trisomy 11.

P. Cin, H. Berghe, H. van den Berghe, 1998, Cancer genetics and cytogenetics.

Peripheral primitive neuroectodermal tumour of the cervix

P. D. Dal Cin, P. Pauwels, P. Ambros, 2000, Virchows Archiv.

Design of a Special Interpreter for the Classification of Human Chromosomes

A. Oosterlinck, H. Berghe, L. Vanderheydt, 1979, IEEE Trans. Pattern Anal. Mach. Intell..

The effects of changes in the funding structure of the Flemish universities on their research capacity, productivity and impact during the 1980's and early 1990's

Henk F. Moed, Marc Luwel, Eric H. J. Spruyt, 1998, Scientometrics.

Sister chromatid exchange frequencies in cultured human cells exposed to an organophosphorus insecticide: Dichlorvos

H. Berghe, A. H. Nicholas, M. Vienne, 1978 .

Statistical evaluation of sister chromatid exchanges

R. Vlietinck, J. Cassiman, H. Berghe, 2004, Human Genetics.

Aniridia-Wilms' tumor association and 11p interstitial deletion

J. Fryns, H. Berghe, J. François, 1981, European Journal of Pediatrics.

A CYTOGENETIC ANOMALY ASSOCIATED WITH B-CELL LYMPHOMAS OF NON-FOLLICLE CENTRE

C. Wolf‐Peeters, C. Mecucci, M. Stul, 2005 .

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

H. Berghe, F. Baets, 2022 .