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Results: 1-25 | 26-29
Results: 1-25/29
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
A NEAR FALSE-NEGATIVE FINDING OF MOSAIC TRISOMY-21 - A CAUTIONARY TALE
Authors: BEVERSTOCK GC HANSSON K HELDERMANVANDENENDEN TJM BROCKERVRIENDS A KLUMPER F BARTELINGS M DOBBEVANMEERENDONK W ROOSMALEN JV KOLKMAN PH KANHAI HHH
Citation: Gc. Beverstock et al., A NEAR FALSE-NEGATIVE FINDING OF MOSAIC TRISOMY-21 - A CAUTIONARY TALE, Prenatal diagnosis, 18(7), 1998, pp. 742-746
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
MOSAICISM OF THE 5Q DELETION AS ASSESSED BY INTERPHASE FISH IS A COMMON PHENOMENON IN MDS AND RESTRICTED TO MYELOID CELLS
Authors: KROEF MJPL BOLK MJW MUUS P WESSELS JW BEVERSTOCK GC WILLEMZE R LANDEGENT JE
Citation: Mjpl. Kroef et al., MOSAICISM OF THE 5Q DELETION AS ASSESSED BY INTERPHASE FISH IS A COMMON PHENOMENON IN MDS AND RESTRICTED TO MYELOID CELLS, Leukemia, 11(4), 1997, pp. 519-523
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
A NEAR FALSE-NEGATIVE FINDING OF MOSAIC TRISOMY-21 - A CAUTIONARY TALE
Authors: BEVERSTOCK GC HELDERMAN A KLUMPER F BARTELINGS M VANROOSMALEN J KOLKMAN PH KANHAI HHH
Citation: Gc. Beverstock et al., A NEAR FALSE-NEGATIVE FINDING OF MOSAIC TRISOMY-21 - A CAUTIONARY TALE, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 140-140
YET ANOTHER VARIATION ON THE THEME OF CHROMOSOME-18 HETEROMORPHISMS
Authors: BEVERSTOCK GC KLUMPER F VANDERENDEN ATJMH
Citation: Gc. Beverstock et al., YET ANOTHER VARIATION ON THE THEME OF CHROMOSOME-18 HETEROMORPHISMS, Prenatal diagnosis, 17(6), 1997, pp. 585-586
PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER-DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION T(17-20) (P13.3-Q13.3) DETECTED BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: VANZELDERENBHOLA SL BRESLAUSIDERIUS EJ BEVERSTOCK GC STOLTEDIJKSTRA I DEVRIES LS DEPATER JM
Citation: Sl. Vanzelderenbhola et al., PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER-DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION T(17-20) (P13.3-Q13.3) DETECTED BY FLUORESCENCE IN-SITU HYBRIDIZATION, Prenatal diagnosis, 17(2), 1997, pp. 173-179
A 2ND CASE OF HEXASOMY-8 IN MYELODYSPLASTIC SYNDROME
Authors: BEVERSTOCK GC WESSELS HW MOLLEVANGER P DENOTTOLANDER GJ GOTTLIEB DJ
Citation: Gc. Beverstock et al., A 2ND CASE OF HEXASOMY-8 IN MYELODYSPLASTIC SYNDROME, Cancer genetics and cytogenetics, 99(1), 1997, pp. 68-72
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
SIMPLE METHOD FOR DETECTION OF MYH11 DNA REARRANGEMENTS IN PATIENTS WITH INV(16)(P13Q22) AND ACUTE MYELOID-LEUKEMIA
Authors: VANDERREIJDEN BA MARTINET D DAUWERSE JG GILES RH WESSELS JW BEVERSTOCK GC SMIT B MUHLEMATTER D BELLOMO MJ GABERT J LAFAGEPOCHITALOFF M REIFFERS J BILHOUNABERA C VANOMMEN GJB HAGEMEIJER A BREUNING MH
Citation: Ba. Vanderreijden et al., SIMPLE METHOD FOR DETECTION OF MYH11 DNA REARRANGEMENTS IN PATIENTS WITH INV(16)(P13Q22) AND ACUTE MYELOID-LEUKEMIA, Leukemia, 10(9), 1996, pp. 1459-1462
DETECTION OF FETAL ERYTHROBLASTS IN MATERNAL BLOOD BY ONESTEP GRADIENT ENRICHMENT AND IMMUNOCYTOCHEMICAL RECOGNITION
Authors: OOSTERWIJK JC MESKER WE OUWERKERK MCM KNEPFLE CFHM VANDERBURG MJM WIESMEIJER CC BEVERSTOCK GC LOSEKOOT M BERNINI LF VANOMMEN GJB VANDEKAMP JJP KANHAI HHH TANKE HJ
Citation: Jc. Oosterwijk et al., DETECTION OF FETAL ERYTHROBLASTS IN MATERNAL BLOOD BY ONESTEP GRADIENT ENRICHMENT AND IMMUNOCYTOCHEMICAL RECOGNITION, Early human development, 47, 1996, pp. 95-97
CONSTRUCTION OF A 850-KB COSMID CONTIG SURROUNDING THE CBP GENE, INVOLVED IN RUBINSTEIN-TAYBI SYNDROME AND ANLL M4 M5 WITH T(8-16)(P11-P13.3)/
Authors: GILES RH PETRIJ F DAUWERSE JG BEVERSTOCK GC HAGEMEIJER A PETERS DJM BREUNING MH
Citation: Rh. Giles et al., CONSTRUCTION OF A 850-KB COSMID CONTIG SURROUNDING THE CBP GENE, INVOLVED IN RUBINSTEIN-TAYBI SYNDROME AND ANLL M4 M5 WITH T(8-16)(P11-P13.3)/, Cytogenetics and cell genetics, 72(4), 1996, pp. 12-12
A CASE OF ISODICENTRIC 7P AS SOLE ABNORMALITY IN A PATIENT WITH ACUTEMYELOID-LEUKEMIA
Authors: BEVERSTOCK GC DEMEIJER PHEM HUININK DT PRUIJT JFM DENOTTOLANDER GJ WESSELS HW MOLLEVANGER P
Citation: Gc. Beverstock et al., A CASE OF ISODICENTRIC 7P AS SOLE ABNORMALITY IN A PATIENT WITH ACUTEMYELOID-LEUKEMIA, Cancer genetics and cytogenetics, 89(2), 1996, pp. 132-135
MOLECULAR, CYTOGENETIC, AND PHENOTYPIC STUDIES OF A CONSTITUTIONAL RECIPROCAL TRANSLOCATION T(5-10)(Q22-Q25) RESPONSIBLE FOR FAMILIAL ADENOMATOUS POLYPOSIS IN A DUTCH PEDIGREE
Authors: VANDERLUIJT RB TOPS CMJ KHAN PM VANDERKLIFT HM BREUKEL C VANLEEUWENCORNELISSE ISJ DAUWERSE HG BEVERSTOCK GC VANNOORT E SNEL P SLORS FJM VASEN HFA FODDE R
Citation: Rb. Vanderluijt et al., MOLECULAR, CYTOGENETIC, AND PHENOTYPIC STUDIES OF A CONSTITUTIONAL RECIPROCAL TRANSLOCATION T(5-10)(Q22-Q25) RESPONSIBLE FOR FAMILIAL ADENOMATOUS POLYPOSIS IN A DUTCH PEDIGREE, Genes, chromosomes & cancer, 13(3), 1995, pp. 192-202
CEREBELLAR AND BRAIN-STEM HYPOPLASIA IN A CHILD WITH A PARTIAL MONOSOMY FOR THE SHORT ARM OF CHROMOSOME-5 AND PARTIAL TRISOMY FOR THE SHORTARM OF CHROMOSOME-10
Authors: ARTS WFM HOFSTEE Y DREJER GF BEVERSTOCK GC OOSTERWIJK JC
Citation: Wfm. Arts et al., CEREBELLAR AND BRAIN-STEM HYPOPLASIA IN A CHILD WITH A PARTIAL MONOSOMY FOR THE SHORT ARM OF CHROMOSOME-5 AND PARTIAL TRISOMY FOR THE SHORTARM OF CHROMOSOME-10, Neuropediatrics, 26(1), 1995, pp. 41-44
THE TRANSLOCATION T(8-16) IN ANLL M4 M5 DISRUPTS THE CBP GENE ON CHROMOSOME-16/
Authors: GILES RH PETRIJ F DAUWERSE JG VANDERREIJDEN BA BEVERSTOCK GC HAGEMEIJER A BREUNING MH
Citation: Rh. Giles et al., THE TRANSLOCATION T(8-16) IN ANLL M4 M5 DISRUPTS THE CBP GENE ON CHROMOSOME-16/, Blood, 86(10), 1995, pp. 128-128
DELETION OF 11Q13 REARRANGEMENTS IN HEMATOLOGIC MALIGNANCIES BY DOUBLE COLOR FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: COIGNET LJA SCHUURING E KIBBELAAR RE RAAP AK KLEIVERDA JK BERTHEAS MF WIEGANT J BEVERSTOCK GC KLUIN PM
Citation: Lja. Coignet et al., DELETION OF 11Q13 REARRANGEMENTS IN HEMATOLOGIC MALIGNANCIES BY DOUBLE COLOR FLUORESCENCE IN-SITU HYBRIDIZATION, Blood, 86(10), 1995, pp. 1361-1361
CYTOGENETIC ANALYSIS OF MULTIPLE-MYELOMA
Authors: HAAK HL WIJERMANS PW VONWEERT J BEVERSTOCK GC
Citation: Hl. Haak et al., CYTOGENETIC ANALYSIS OF MULTIPLE-MYELOMA, Blood, 86(10), 1995, pp. 3322-3322
RT-PCR DIAGNOSIS OF PATIENTS WITH ACUTE NONLYMPHOCYTIC LEUKEMIA AND INV(16)(P13Q22) AND IDENTIFICATION OF NEW ALTERNATIVE SPLICING IN CBFB-MYH11 TRANSCRIPTS
Authors: VANDERREIJDEN BA LOMBARDO M DAUWERSE HG GILES RH MUHLEMATTER D BELLOMO MJ WESSELS HW BEVERSTOCK GC VANOMMEN GJB HAGEMEIJER A BREUNING MH
Citation: Ba. Vanderreijden et al., RT-PCR DIAGNOSIS OF PATIENTS WITH ACUTE NONLYMPHOCYTIC LEUKEMIA AND INV(16)(P13Q22) AND IDENTIFICATION OF NEW ALTERNATIVE SPLICING IN CBFB-MYH11 TRANSCRIPTS, Blood, 86(1), 1995, pp. 277-282
PROLIFERATION AND CYTOGENETIC ANALYSIS OF HAIRY-CELL LEUKEMIA UPON STIMULATION VIA THE CD40 ANTIGEN
Authors: KLUINNELEMANS HC BEVERSTOCK GC MOLLEVANGER P WESSELS HW HOOGENDOORN E WILLEMZE R FALKENBURG JHF
Citation: Hc. Kluinnelemans et al., PROLIFERATION AND CYTOGENETIC ANALYSIS OF HAIRY-CELL LEUKEMIA UPON STIMULATION VIA THE CD40 ANTIGEN, Blood, 84(9), 1994, pp. 3134-3141
PROLIFERATION AND CYTOGENETIC ANALYSIS OF HAIRY-CELL LEUKEMIA UPON STIMULATION VIA THE CD40 ANTIGEN
Authors: KLUINNELEMANS HC BEVERSTOCK GC MOLLEVANGER P WESSELS HW HOOGENDOORN E WILLEMZE R FALKENBURG JHF
Citation: Hc. Kluinnelemans et al., PROLIFERATION AND CYTOGENETIC ANALYSIS OF HAIRY-CELL LEUKEMIA UPON STIMULATION VIA THE CD40 ANTIGEN, Blood, 84(9), 1994, pp. 3134-3141
CLONING THE BREAKPOINT CLUSTER REGION OF THE INV(16) IN ACUTE NONLYMPHOCYTIC LEUKEMIA M4 EO
Authors: DAUWERSE JG WESSELS JW GILES RH WIEGANT J VANDERREIJDEN BA FUGAZZA G JUMELET EA SMIT E BAAS F RAAP AK HAGEMEIJER A BEVERSTOCK GC VANOMMEN GJB BREUNING MH
Citation: Jg. Dauwerse et al., CLONING THE BREAKPOINT CLUSTER REGION OF THE INV(16) IN ACUTE NONLYMPHOCYTIC LEUKEMIA M4 EO, Human molecular genetics, 2(10), 1993, pp. 1527-1534
Risultati: 1-25 | 26-29