AAAAAA

   
Results: 1-25 | 26-47
Results: 1-25/47
POLYMORPHIC DETECTION OF A PARTHENOGENETIC MATERNAL AND DOUBLE PATERNAL CONTRIBUTION TO A 46,XX 46,XY HERMAPHRODITE/
Authors: GILTAY JC BRUNT T BEEMER FA WIT JM VANAMSTEL HKP PEARSON PL WIJMENGA C
Citation: Jc. Giltay et al., POLYMORPHIC DETECTION OF A PARTHENOGENETIC MATERNAL AND DOUBLE PATERNAL CONTRIBUTION TO A 46,XX 46,XY HERMAPHRODITE/, American journal of human genetics, 62(4), 1998, pp. 937-940
LOCALIZATION OF ICF SYNDROME BY HOMOZYGOSITY MAPPING
Authors: WIJMENGA C VANDENHEUVEL L STRENGMAN E LUYTEN J VANDERBURGT I DEGROOT R SMEETS D VANDONGEN J PEARSON P SANDKUIJL L WEEMAES C
Citation: C. Wijmenga et al., LOCALIZATION OF ICF SYNDROME BY HOMOZYGOSITY MAPPING, Molecular immunology, 35(11-12), 1998, pp. 719-719
LOCALIZATION OF THE ICF SYNDROME TO CHROMOSOME-20 BY HOMOZYGOSITY MAPPING
Authors: WIJMENGA C VANDENHEUVEL LPWJ STRENGMAN E LUYTEN JAFM VANDERBURGT IJAM DEGROOT R SMEETS DFCM DRAAISMA JMT VANDONGEN JJ DEABREU RA PEARSON PL SANDKUIJL LA WEEMAES CMR
Citation: C. Wijmenga et al., LOCALIZATION OF THE ICF SYNDROME TO CHROMOSOME-20 BY HOMOZYGOSITY MAPPING, American journal of human genetics, 63(3), 1998, pp. 803-809
IDENTIFICATION OF THE CHIMERIC PROTEIN PRODUCT OF THE CBFB-MYH11 FUSION GENE IN INV(16) LEUKEMIA-CELLS (VOL 16, PG 77, 1996)
Authors: PAUL LP WIJMENGA C HAJRA A BLAKE TB KELLEY CA ADELSTEIN RS BAGG A RECTOR J COTELLINGAM J WILLMAN CL COLLINS FS
Citation: Lp. Paul et al., IDENTIFICATION OF THE CHIMERIC PROTEIN PRODUCT OF THE CBFB-MYH11 FUSION GENE IN INV(16) LEUKEMIA-CELLS (VOL 16, PG 77, 1996), Genes, chromosomes & cancer, 18(1), 1997, pp. 71-71
ISOCHROMOSOME 1Q AS THE SOLE CHROMOSOMAL ABNORMALITY IN FETAL TERATOMAS
Authors: SCHERES J DEPATER J VISSERS J WIJMENGA C PEARSON P DULLENS H STOUTENBEEK P ESSED C KNOL I
Citation: J. Scheres et al., ISOCHROMOSOME 1Q AS THE SOLE CHROMOSOMAL ABNORMALITY IN FETAL TERATOMAS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 381-381
THE ENDEMIC TYROLEAN INFANTILE CIRRHOSIS LOCUS IS NOT ON 13Q14.3, THEWILSON DISEASE LOCUS
Authors: HOUWEN RHJ MULLER T BRUNT T FEICHTINGER H MULLER W SANDKUIJL LA PEARSON PL WIJMENGA C
Citation: Rhj. Houwen et al., THE ENDEMIC TYROLEAN INFANTILE CIRRHOSIS LOCUS IS NOT ON 13Q14.3, THEWILSON DISEASE LOCUS, Hepatology, 26(4), 1997, pp. 1591-1591
ANALYSIS OF DNA POLYMORPHISMS IN A PATIENT WITH AMBIGUOUS GENITALIA AND A 46,XX 46,XY MOSAICISM SUGGESTS A HAPLOID MATERNAL GENETIC CONTRIBUTION/
Authors: GILTAY JC BRUNT T BEEMER FA WIT JM VANAMSTEL HKP PEARSON PL WIJMENGA C
Citation: Jc. Giltay et al., ANALYSIS OF DNA POLYMORPHISMS IN A PATIENT WITH AMBIGUOUS GENITALIA AND A 46,XX 46,XY MOSAICISM SUGGESTS A HAPLOID MATERNAL GENETIC CONTRIBUTION/, American journal of human genetics, 61(4), 1997, pp. 716-716
THE ENDEMIC TYROLEAN INFANTILE CIRRHOSIS LOCUS IS NOT LINKED TO THE WND LOCUS ON CHROMOSOME-13
Authors: WIJMENGA C MULLER T BRUNT T FEICHTIGER H SCHONITZER D HOUWEN R MULLER W SANDKUIJL LA PEARSON PL
Citation: C. Wijmenga et al., THE ENDEMIC TYROLEAN INFANTILE CIRRHOSIS LOCUS IS NOT LINKED TO THE WND LOCUS ON CHROMOSOME-13, American journal of human genetics, 61(4), 1997, pp. 2360-2360
IDENTIFICATION OF THE CHIMERIC PROTEIN PRODUCT OF THE CBFB-MYHII FUSION GENE IN INV(16) LEUKEMIA-CELLS
Authors: LIU PP WIJMENGA C HAJRA A BLAKE TB KELLEY CA ADELSTEIN RS BAGG A RECTOR J COTELINGAM J WILLMAN CL COLLINS FS
Citation: Pp. Liu et al., IDENTIFICATION OF THE CHIMERIC PROTEIN PRODUCT OF THE CBFB-MYHII FUSION GENE IN INV(16) LEUKEMIA-CELLS, Genes, chromosomes & cancer, 16(2), 1996, pp. 77-87
FAILURE OF EMBRYONIC HEMATOPOIESIS AND LETHAL HEMORRHAGES IN MOUSE EMBRYOS HETEROZYGOUS FOR A KNOCKED-IN LEUKEMIA GENE CBFB-MYH11
Authors: CASTILLA LH WIJMENGA C WANG Q STACY T SPECK NA ECKHAUS M MARINPADILLA M COLLINS FS WYNSHAWBORIS A LIU PP
Citation: Lh. Castilla et al., FAILURE OF EMBRYONIC HEMATOPOIESIS AND LETHAL HEMORRHAGES IN MOUSE EMBRYOS HETEROZYGOUS FOR A KNOCKED-IN LEUKEMIA GENE CBFB-MYH11, Cell, 87(4), 1996, pp. 687-696
CORE BINDING-FACTOR BETA-SMOOTH MUSCLE MYOSIN HEAVY-CHAIN CHIMERIC PROTEIN INVOLVED IN ACUTE MYELOID-LEUKEMIA FORMS UNUSUAL NUCLEAR ROD-LIKE STRUCTURES IN TRANSFORMED NIH 3T3 CELLS
Authors: WIJMENGA C GREGORY PE HAJRA A SCHROCK E RIED T EILS R LIU PP COLLINS FS
Citation: C. Wijmenga et al., CORE BINDING-FACTOR BETA-SMOOTH MUSCLE MYOSIN HEAVY-CHAIN CHIMERIC PROTEIN INVOLVED IN ACUTE MYELOID-LEUKEMIA FORMS UNUSUAL NUCLEAR ROD-LIKE STRUCTURES IN TRANSFORMED NIH 3T3 CELLS, Proceedings of the National Academy of Sciences of the United Statesof America, 93(4), 1996, pp. 1630-1635
CORE BINDING-FACTOR BETA-SMOOTH MUSCLE MYOSIN HEAVY-CHAIN CHIMERIC PROTEIN INVOLVED IN ACUTE MYELOID-LEUKEMIA FORMS UNUSUAL NUCLEAR ROD-LIKE STRUCTURES IN TRANSFORMED NIH 3T3 CELLS (VOL 93, PG 1630, 1996)
Authors: WIJMENGA C GREGORY PE HAJRA A SCHROCK E RIED T EILS R LIU PP COLLINS FS
Citation: C. Wijmenga et al., CORE BINDING-FACTOR BETA-SMOOTH MUSCLE MYOSIN HEAVY-CHAIN CHIMERIC PROTEIN INVOLVED IN ACUTE MYELOID-LEUKEMIA FORMS UNUSUAL NUCLEAR ROD-LIKE STRUCTURES IN TRANSFORMED NIH 3T3 CELLS (VOL 93, PG 1630, 1996), Proceedings of the National Academy of Sciences of the United Statesof America, 93(26), 1996, pp. 15522-15522
DIAGNOSTIC, PREDICTIVE, AND PRENATAL TESTING FOR FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY - DIAGNOSTIC-APPROACH FOR SPORADIC AND FAMILIAL CASES
Authors: BAKKER E VANDERWIELEN MJR VOORHOEVE E IPPEL PF PADBERG GW FRANTS RR WIJMENGA C
Citation: E. Bakker et al., DIAGNOSTIC, PREDICTIVE, AND PRENATAL TESTING FOR FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY - DIAGNOSTIC-APPROACH FOR SPORADIC AND FAMILIAL CASES, Journal of Medical Genetics, 33(1), 1996, pp. 29-35
GERMLINE TRANSMISSION OF THE LEUKEMIA FUSION GENE CBFB-MYH11 CAUSES BLOCKAGE OF DEFINITIVE HEMATOPOIESIS AND EMBRYONIC LETHAL HEMORRHAGE INHETEROZYGOUS (CBFB-MYH11 + -) EMBRYOS/
Authors: CASTILLA LH WIJMENGA C WANG Q SPECK NA COLLINS FS WYNSHAWBORIS A LIU PP
Citation: Lh. Castilla et al., GERMLINE TRANSMISSION OF THE LEUKEMIA FUSION GENE CBFB-MYH11 CAUSES BLOCKAGE OF DEFINITIVE HEMATOPOIESIS AND EMBRYONIC LETHAL HEMORRHAGE INHETEROZYGOUS (CBFB-MYH11 + -) EMBRYOS/, Blood, 88(10), 1996, pp. 1149-1149
IDENTIFICATION OF A NEW MURINE RUNT DOMAIN-CONTAINING GENE, CBFA3, AND LOCALIZATION OF THE HUMAN HOMOLOG, CBFA3, TO CHROMOSOME 1P35-PTER
Authors: WIJMENGA C SPECK NA DRACOPOLI NC HOFKER MH LIU P COLLINS FS
Citation: C. Wijmenga et al., IDENTIFICATION OF A NEW MURINE RUNT DOMAIN-CONTAINING GENE, CBFA3, AND LOCALIZATION OF THE HUMAN HOMOLOG, CBFA3, TO CHROMOSOME 1P35-PTER, Genomics, 26(3), 1995, pp. 611-614
ANALYSIS OF THE FUSION GENE GENERATED BY CHROMOSOME-16 INVERSION IN LEUKEMIA
Authors: LIU P HAJRA A GREGORY P WIJMENGA C BLAKE T COLLINS F
Citation: P. Liu et al., ANALYSIS OF THE FUSION GENE GENERATED BY CHROMOSOME-16 INVERSION IN LEUKEMIA, Journal of cellular biochemistry, 1995, pp. 69-69
FISH MAPPING OF 250 COSMID AND 26 YAC CLONES TO CHROMOSOME-4 WITH SPECIAL EMPHASIS ON THE FSHD REGION AT 4Q35
Authors: WIJMENGA C DAUWERSE HG PADBERG GW MEYER N MURRAY JC MILLS K VANOMMEN GB HOFKER MH FRANTS RR
Citation: C. Wijmenga et al., FISH MAPPING OF 250 COSMID AND 26 YAC CLONES TO CHROMOSOME-4 WITH SPECIAL EMPHASIS ON THE FSHD REGION AT 4Q35, Muscle & nerve, 1995, pp. 14-18
SEARCH FOR THE FSHD GENE USING CDNA SELECTION IN A REGION SPANNING 100-KB ON CHROMOSOME-4Q35
Authors: VANDEUTEKOM JCT HOFKER MH ROMBERG S VANGEEL M ROMMENS J WRIGHT TJ HEWITT JE PADBERG GW WIJMENGA C FRANTS RR
Citation: Jct. Vandeutekom et al., SEARCH FOR THE FSHD GENE USING CDNA SELECTION IN A REGION SPANNING 100-KB ON CHROMOSOME-4Q35, Muscle & nerve, 1995, pp. 19-26
THE FSHD-LINKED LOCUS D4F104S1 (P13E-11) ON 4Q35 HAS A HOMOLOG ON 10QTER
Authors: BAKKER E WIJMENGA C VOSSEN RHAM PADBERG GW HEWITT J VANDERWIELEN M RASMUSSEN K FRANTS RR
Citation: E. Bakker et al., THE FSHD-LINKED LOCUS D4F104S1 (P13E-11) ON 4Q35 HAS A HOMOLOG ON 10QTER, Muscle & nerve, 1995, pp. 39-44
EARLY-ONSET FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY
Authors: BROUWER OF PADBERG GW BAKKER E WIJMENGA C FRANTS RR
Citation: Of. Brouwer et al., EARLY-ONSET FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY, Muscle & nerve, 1995, pp. 67-72
ON THE SIGNIFICANCE OF RETINAL VASCULAR-DISEASE AND HEARING-LOSS IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY
Authors: PADBERG GW BROUWER OF DEKEIZER RJW DIJKMAN G WIJMENGA C GROTE JJ FRANTS RR
Citation: Gw. Padberg et al., ON THE SIGNIFICANCE OF RETINAL VASCULAR-DISEASE AND HEARING-LOSS IN FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY, Muscle & nerve, 1995, pp. 73-80
FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY IN THE DUTCH POPULATION
Authors: PADBERG GW FRANTS RR BROUWER OF WIJMENGA C BAKKER E SANDKUIJL LA
Citation: Gw. Padberg et al., FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY IN THE DUTCH POPULATION, Muscle & nerve, 1995, pp. 81-84
ANALYSIS OF CBFB-MYH11, THE FUSION GENE PRODUCED BY CHROMOSOME-16 INVERSION IN HUMAN LEUKEMIAS
Authors: WIJMENGA C HAJRA A ADYA N BLAKE T GREGORY P COLLINS FS LIU PP
Citation: C. Wijmenga et al., ANALYSIS OF CBFB-MYH11, THE FUSION GENE PRODUCED BY CHROMOSOME-16 INVERSION IN HUMAN LEUKEMIAS, Blood, 86(10), 1995, pp. 163-163
CLUSTERING OF GENOMIC INV(16)(P13Q22) BREAKPOINTS IN ACUTE NONLYMPHOCYTIC LEUKEMIA
Authors: VANDERREIJDEN BA WIJMENGA C LIU P DAUWERSE JG GILES RH CHANGUR S VANOMMEN GJ HAGEMEIJER A BREUNING M
Citation: Ba. Vanderreijden et al., CLUSTERING OF GENOMIC INV(16)(P13Q22) BREAKPOINTS IN ACUTE NONLYMPHOCYTIC LEUKEMIA, Blood, 86(10), 1995, pp. 2968-2968
MOLECULAR PATHOGENESIS OF THE CHROMOSOME-16 INVERSION IN THE M4EO SUBTYPE OF ACUTE MYELOID-LEUKEMIA
Authors: LIU PP HAJRA A WIJMENGA C COLLINS FS
Citation: Pp. Liu et al., MOLECULAR PATHOGENESIS OF THE CHROMOSOME-16 INVERSION IN THE M4EO SUBTYPE OF ACUTE MYELOID-LEUKEMIA, Blood, 85(9), 1995, pp. 2289-2302
Risultati: 1-25 | 26-47