AAAAAA

   
Results: 1-25 | 26-50 | 51-75 | 76-100 | >>
Results: 1-25/116
THE HUMAN GENOME PROJECT AND THE ROLE OF GENETICS IN HEALTH-CARE
Authors: VANOMMEN GJB
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
FETAL CELL DETECTION IN MATERNAL BLOOD - A MULTIPARAMETER STUDY IN 236 SAMPLES USING ERYTHROBLAST MORPHOLOGY, DAB AND HBF STAINING AND FISHANALYSIS
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
ANALYSIS OF A DEVELOPMENTAL GENE DELETED IN PATIENTS WITH WOLF-HIRSCHHORN-SYNDROME
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
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
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
FUNCTIONAL IMPLICATIONS OF THE SPECTRUM OF MUTATIONS FOUND IN 234 CASES WITH X-LINKED JUVENILE RETINOSCHISIS (XLRS)
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
CLINICAL-DIAGNOSIS OF HETEROZYGOUS DYSTROPHIN GENE DELETIONS BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: ROSENBERG C NAVAJAS L VAGENAS DF BAKKER E VAINZOF M PASSOSBUENO MR TAKATA RI VANOMMEN GJB ZATZ M 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
CHARACTERIZATION OF SCML1, A NEW GENE IN XP22, WITH HOMOLOGY TO DEVELOPMENTAL POLYCOMB GENES
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 VANOMMEN GJB 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
2-COLOR IMMUNOCYTOCHEMICAL STAINING OF GAMMA (GAMMA) AND EPSILON (EPSILON) TYPE HEMOGLOBIN IN FETAL RED-CELLS
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
PRENATAL-DIAGNOSIS OF TRISOMY-13 ON FETAL CELLS OBTAINED FROM MATERNAL BLOOD AFTER MINOR ENRICHMENT
Authors: OOSTERWIJK JC MESKER WE OUWERKERKVANVELZEN MCM KNEPFLE CFHM WIESMEIJER KC BEVERSTOCK GC VANOMMEN GJB TANKE HJ KANHAI HHH
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
DEVELOPMENT OF A PREPARATION AND STAINING METHOD FOR FETAL ERYTHROBLASTS IN MATERNAL BLOOD - SIMULTANEOUS IMMUNOCYTOCHEMICAL STAINING AND FISH ANALYSIS
Authors: OOSTERWIJK JC MESKER WE OUWERKERKVANVELZEN MCM KNEPFLE CFHM WIESMEIJER KC VANDENBURG MJM BEVERSTOCK GC BERNINI LF VANOMMEN GJB KANHAI HHH TANKE HJ
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
FETAL CELL DETECTION IN MATERNAL BLOOD - A STUDY IN 236 SAMPLES USINGERYTHROBLAST MORPHOLOGY, DAB AND HBF STAINING, AND FISH ANALYSIS
Authors: OOSTERWIJK JC MESKER WE OUWERKERKVANVELZEN MCM KNEPFLE CFHM WIESMEIJER KC BEVERSTOCK GC VANOMMEN GJB KANHAI HHH TANKE HJ
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
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
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
DO HUMAN CHROMOSOMAL BANDS 16P13 AND 22Q11-13 SHARE ANCESTRAL ORIGINS
Authors: GILES RH DAUWERSE HG VANOMMEN GJB BREUNING MH
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
FOUNDER EFFECT AT PGL1 IN HEREDITARY HEAD AND NECK PARAGANGLIOMA FAMILIES FROM THE NETHERLANDS
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
BRCA1 GENOMIC DELETIONS ARE MAJOR FOUNDER MUTATIONS IN DUTCH BREAST-CANCER PATIENTS
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
CENTROMERIC AND NONCENTROMERIC ADE2-SELECTABLE FRAGMENTATION VECTORS FOR YEAST ARTIFICIAL CHROMOSOMES IN AB1380
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
UNTITLED
Authors: VANOMMEN GJB
Citation: Gjb. Vanommen, UNTITLED, European journal of human genetics, 5(4), 1997, pp. 179-179
HIGH-RESOLUTION MAPPING BY YAC FRAGMENTATION OF A 2.5-MB XP22 REGION CONTAINING THE HUMAN RS, KFSD AND CLS DISEASE GENES
Authors: VANDEVOSSE E VANDERBENT P HEUS JJ VANOMMEN GJB 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
CONSTRUCTION OF A 1.2-MB CONTIG SURROUNDING, AND MOLECULAR ANALYSIS OF, THE HUMAN CREB-BINDING PROTEIN (CBP CREBBP) GENE ON CHROMOSOME 16P13.3/
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
DETECTION OF CBP REARRANGEMENTS IN ACUTE MYELOGENOUS LEUKEMIA WITH T(8-16)
Authors: GILES RH DAUWERSE JG HIGGINS C PETRIJ F WESSELS JW BEVERSTOCK GC DOHNER H JOTTERANDBELLOMO M FALKENBURG JHF SLATER RM VANOMMEN GJB 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
EXCLUSION OF PPEF AS THE GENE CAUSING X-LINKED JUVENILE RETINOSCHISIS
Authors: VANDEVOSSE E FRANCO B VANDERBENT P MONTINI E ORTH U HANAUER A TIJMES N VANOMMEN GJB BALLABIO A DENDUNNEN JT BERGEN AAB
Citation: E. Vandevosse et al., EXCLUSION OF PPEF AS THE GENE CAUSING X-LINKED JUVENILE RETINOSCHISIS, Human genetics, 101(2), 1997, pp. 235-237
MOLECULAR-GENETIC ANALYSIS OF 2 FAMILIES WITH KERATOSIS-FOLLICULARIS SPINULOSA DECALVANS - REFINEMENT OF GENE LOCALIZATION AND EVIDENCE FORGENETIC-HETEROGENEITY
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
EVOLUTION OF CARDIAC ABNORMALITIES IN BECKER MUSCULAR-DYSTROPHY OVER A 13-YEAR PERIOD
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
PITT-ROGERS-DANKS-SYNDROME AND WOLF-HIRSCHHORN-SYNDROME ARE CAUSED BYA DELETION IN THE SAME REGION ON CHROMOSOME 4P16.3
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
THE CLINICAL AND MOLECULAR-GENETIC APPROACH TO DUCHENNE AND BECKER MUSCULAR-DYSTROPHY - AN UPDATED PROTOCOL
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
Risultati: 1-25 | 26-50 | 51-75 | 76-100 | >>