Citation: Gjb. Vanommen, THE HUMAN GENOME PROJECT AND THE ROLE OF GENETICS IN HEALTH-CARE, CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 36(8), 1998, pp. 515-517
Authors:
OOSTERWIJK JC
MESKER WE
OUWERKERKVANVELZEN MCM
KNEPFLE CFHM
WIESMEIJER CC
BEVERSTOCK GC
VANOMMEN GJB
TANKE HJ
KANHAI HHH
Citation: Jc. Oosterwijk et al., FETAL CELL DETECTION IN MATERNAL BLOOD - A MULTIPARAMETER STUDY IN 236 SAMPLES USING ERYTHROBLAST MORPHOLOGY, DAB AND HBF STAINING AND FISHANALYSIS, European journal of human genetics, 6, 1998, pp. 2030-2030
Authors:
STEC I
DENDUNNEN JT
WRIGHT TJ
DEBOER PAJ
VANHAERINGEN A
MOORMAN AFM
ALTHERR MR
DONNAI D
CROQUETTE MF
TOUTAIN A
VANOMMEN GJB
Citation: I. Stec et al., ANALYSIS OF A DEVELOPMENTAL GENE DELETED IN PATIENTS WITH WOLF-HIRSCHHORN-SYNDROME, European journal of human genetics, 6, 1998, pp. 6040-6040
Authors:
STEC I
WRIGHT TJ
VANOMMEN GJB
DEBOER PAJ
VANHAERINGEN A
MOORMAN AFM
ALTHERR MR
DENDUNNEN JT
Citation: I. Stec et al., WHSC1, A 90 KB SET DOMAIN-CONTAINING GENE, EXPRESSED IN EARLY DEVELOPMENT AND HOMOLOGOUS TO A DROSOPHILA DYSMORPHY GENE MAPS IN THE WOLF-HIRSCHHORN-SYNDROME CRITICAL REGION AND IS FUSED TO IGH IN T(4-14) MULTIPLE-MYELOMA, Human molecular genetics (Print), 7(7), 1998, pp. 1071-1082
Authors:
DENDUNNEN JT
KRAAYENBRINK T
VANSCHOONEVELD M
VANDEVOSSE E
DEJONG PTVM
TENBRINK JB
SCHUURMAN E
TIJMES N
VANOMMEN GJB
BERGEN AAB
ANDOLFI G
MONTINI E
LI Y
OUDET C
BOLZ H
KAPLAN J
ORTH U
GAL A
HANAUER A
BARDELLI AM
AYUSO C
DIAZ FJ
BITOUN P
VENTRUTO V
BALLABIO A
FRANCO B
HIRIYANNA KT
BINGHAM EL
MCHENRY C
PAWAR H
COATS C
DARGA T
RICHARDS JE
SIEVING PA
HUOPANIEMI L
RANTALA A
ROSENBERG T
DAHL N
WRIGHT A
DELACHAPELLE A
ALITALO T
LENZNER S
BRUNNER B
FEIL S
NIESLER B
SCHULZ U
PINCKERS A
BLANKENNAGEL A
RUETHER K
KELLNER U
RAPPOLD G
ROPERS HH
KALSCHEUER V
BERGER W
TRUMP D
WALPOLE SM
NICOLAOU A
GAYTHOR SA
PIMENIDES D
GEORGE NDL
MOORE UT
YATES JRW
Citation: Jt. Dendunnen et al., FUNCTIONAL IMPLICATIONS OF THE SPECTRUM OF MUTATIONS FOUND IN 234 CASES WITH X-LINKED JUVENILE RETINOSCHISIS (XLRS), Human molecular genetics (Print), 7(7), 1998, pp. 1185-1192
Authors:
ROSENBERG C
NAVAJAS L
VAGENAS DF
BAKKER E
VAINZOF M
PASSOSBUENO MR
TAKATA RI
VANOMMEN GJB
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DENDUNNEN JT
Citation: C. Rosenberg et al., CLINICAL-DIAGNOSIS OF HETEROZYGOUS DYSTROPHIN GENE DELETIONS BY FLUORESCENCE IN-SITU HYBRIDIZATION, Neuromuscular disorders, 8(7), 1998, pp. 447-452
Authors:
VANDEVOSSE E
WALPOLE SM
NICOLAOU A
VANDERBENT P
CAHN A
VAUDIN M
ROSS MT
DURHAM J
PAVITT R
WILKINSON J
GRAFHAM D
BERGEN AAB
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YATES JRW
DENDUNNEN JT
TRUMP D
Citation: E. Vandevosse et al., CHARACTERIZATION OF SCML1, A NEW GENE IN XP22, WITH HOMOLOGY TO DEVELOPMENTAL POLYCOMB GENES, Genomics, 49(1), 1998, pp. 96-102
Authors:
MESKER WE
VELZEN MCMOV
OOSTERWIJK JC
BERNINI LF
GOLBUS MS
KANHAI HHH
VANOMMEN GJB
TANKE HJ
Citation: We. Mesker et al., 2-COLOR IMMUNOCYTOCHEMICAL STAINING OF GAMMA (GAMMA) AND EPSILON (EPSILON) TYPE HEMOGLOBIN IN FETAL RED-CELLS, Prenatal diagnosis, 18(11), 1998, pp. 1131-1137
Citation: Jc. Oosterwijk et al., PRENATAL-DIAGNOSIS OF TRISOMY-13 ON FETAL CELLS OBTAINED FROM MATERNAL BLOOD AFTER MINOR ENRICHMENT, Prenatal diagnosis, 18(10), 1998, pp. 1082-1085
Citation: Jc. Oosterwijk et al., DEVELOPMENT OF A PREPARATION AND STAINING METHOD FOR FETAL ERYTHROBLASTS IN MATERNAL BLOOD - SIMULTANEOUS IMMUNOCYTOCHEMICAL STAINING AND FISH ANALYSIS, Cytometry, 32(3), 1998, pp. 170-177
Citation: Jc. Oosterwijk et al., FETAL CELL DETECTION IN MATERNAL BLOOD - A STUDY IN 236 SAMPLES USINGERYTHROBLAST MORPHOLOGY, DAB AND HBF STAINING, AND FISH ANALYSIS, Cytometry, 32(3), 1998, pp. 178-185
Authors:
VANSCHOTHORST EM
BEEKMAN M
TORREMANS P
KUIPERSDIJKSHOORN NJ
WESSELS HW
BARDOEL AFJ
VANDERMEY AGL
VANOMMEN GJB
DEVILEE P
CORNELISSE CJ
Citation: Em. Vanschothorst et al., PARAGANGLIOMAS OF THE HEAD AND NECK REGION SHOW COMPLETE LOSS OF HETEROZYGOSITY AT 11Q22-Q23 IN CHIEF CELLS AND THE FLOW-SORTED DNA ANEUPLOID FRACTION, Human pathology, 29(10), 1998, pp. 1045-1049
Citation: Rh. Giles et al., DO HUMAN CHROMOSOMAL BANDS 16P13 AND 22Q11-13 SHARE ANCESTRAL ORIGINS, American journal of human genetics, 63(4), 1998, pp. 1240-1242
Authors:
VANSCHOTHORST EM
JANSEN JC
GROOTERS E
PRINS DEM
WIERSINGA LJ
VANDERMEY AGL
VANOMMEN GJB
DEVILEE P
CORNELISSE CJ
Citation: Em. Vanschothorst et al., FOUNDER EFFECT AT PGL1 IN HEREDITARY HEAD AND NECK PARAGANGLIOMA FAMILIES FROM THE NETHERLANDS, American journal of human genetics, 63(2), 1998, pp. 468-473
Authors:
PETRIJBOSCH A
PEELEN T
VANVLIET M
VANEIJK R
OLMER R
DRUSEDAU M
HOGERVORST FBL
HAGEMAN S
ARTS PJW
LIGTENBERG MJL
MEIJERSHEIJBOER H
KLIJN JGM
VASEN HFA
CORNELISSE CJ
VANTVEER LJ
BAKKER E
VANOMMEN GJB
DEVILEE P
Citation: A. Petrijbosch et al., BRCA1 GENOMIC DELETIONS ARE MAJOR FOUNDER MUTATIONS IN DUTCH BREAST-CANCER PATIENTS, Nature genetics, 17(3), 1997, pp. 341-345
Authors:
HEUS JJ
DEWINTHER MPJ
VANDEVOSSE E
VANOMMEN GJB
DENDUNNEN JT
Citation: Jj. Heus et al., CENTROMERIC AND NONCENTROMERIC ADE2-SELECTABLE FRAGMENTATION VECTORS FOR YEAST ARTIFICIAL CHROMOSOMES IN AB1380, PCR methods and applications, 7(6), 1997, pp. 657-660
Authors:
VANDEVOSSE E
VANDERBENT P
HEUS JJ
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DENDUNNEN JT
Citation: E. Vandevosse et al., HIGH-RESOLUTION MAPPING BY YAC FRAGMENTATION OF A 2.5-MB XP22 REGION CONTAINING THE HUMAN RS, KFSD AND CLS DISEASE GENES, Mammalian genome, 8(7), 1997, pp. 497-501
Authors:
GILES RH
PETRIJ F
DAUWERSE HG
DENHOLLANDER AI
LUSHNIKOVA T
VANOMMEN GJB
GOODMAN RH
DEAVEN LL
DOGGETT NA
PETERS DJM
BREUNING MH
Citation: Rh. Giles et al., CONSTRUCTION OF A 1.2-MB CONTIG SURROUNDING, AND MOLECULAR ANALYSIS OF, THE HUMAN CREB-BINDING PROTEIN (CBP CREBBP) GENE ON CHROMOSOME 16P13.3/, Genomics, 42(1), 1997, pp. 96-114
Authors:
GILES RH
DAUWERSE JG
HIGGINS C
PETRIJ F
WESSELS JW
BEVERSTOCK GC
DOHNER H
JOTTERANDBELLOMO M
FALKENBURG JHF
SLATER RM
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HAGEMEIJER A
VANDERREIJDEN BA
BREUNING MH
Citation: Rh. Giles et al., DETECTION OF CBP REARRANGEMENTS IN ACUTE MYELOGENOUS LEUKEMIA WITH T(8-16), Leukemia, 11(12), 1997, pp. 2087-2096
Authors:
OOSTERWIJK JC
RICHARD G
VANDERWIELEN MJR
VANDEVOSSE E
HARTH W
SANDKUIJL LA
BAKKER E
VANOMMEN GJB
Citation: Jc. Oosterwijk et al., MOLECULAR-GENETIC ANALYSIS OF 2 FAMILIES WITH KERATOSIS-FOLLICULARIS SPINULOSA DECALVANS - REFINEMENT OF GENE LOCALIZATION AND EVIDENCE FORGENETIC-HETEROGENEITY, Human genetics, 100(5-6), 1997, pp. 520-524
Authors:
HOOGERWAARD EM
DEVOOGT WG
WILDE AAM
VANDERWOUW PA
BAKKER E
VANOMMEN GJB
DEVISSER M
Citation: Em. Hoogerwaard et al., EVOLUTION OF CARDIAC ABNORMALITIES IN BECKER MUSCULAR-DYSTROPHY OVER A 13-YEAR PERIOD, Journal of neurology, 244(10), 1997, pp. 657-663
Authors:
KANT SG
VANHAERINGEN A
BAKKER E
STEC I
DONNAI D
MOLLEVANGER P
BEVERSTOCK GC
LINDEMANKUSSE MC
VANOMMEN GJB
Citation: Sg. Kant et al., PITT-ROGERS-DANKS-SYNDROME AND WOLF-HIRSCHHORN-SYNDROME ARE CAUSED BYA DELETION IN THE SAME REGION ON CHROMOSOME 4P16.3, Journal of Medical Genetics, 34(7), 1997, pp. 569-572
Authors:
VANESSEN AJ
KNEPPERS ALJ
VANDERHOUT AH
SCHEFFER H
GINJAAR IB
TENKATE LP
VANOMMEN GJB
BUYS CHCM
BAKKER E
Citation: Aj. Vanessen et al., THE CLINICAL AND MOLECULAR-GENETIC APPROACH TO DUCHENNE AND BECKER MUSCULAR-DYSTROPHY - AN UPDATED PROTOCOL, Journal of Medical Genetics, 34(10), 1997, pp. 805-812