AAAAAA

   
Results: 1-9 |
Results: 9
IDENTIFICATION OF THE GENE RESPONSIBLE FOR BEST MACULAR DYSTROPHY
Authors: PETRUKHIN K KOISTI MJ BAKALL B LI W XIE GC MARKNELL T SANDGREN O FORSMAN K HOLMGREN G ANDREASSON S VUJIC M BERGEN AAB MCGARTYDUGAN V FIGUEROA D AUSTIN CP METZKER ML CASKEY CT WADELIUS C
Citation: K. Petrukhin et al., IDENTIFICATION OF THE GENE RESPONSIBLE FOR BEST MACULAR DYSTROPHY, Nature genetics, 19(3), 1998, pp. 241-247
CONGENITAL RETT-SYNDROME PHENOTYPE - DELETION SHORT ARM CHROMOSOME-3
Authors: WAHLSTROM J ULLER A TONNBY B DARNFORS C MARTINSSON T VUJIC M HAGBERG B
Citation: J. Wahlstrom et al., CONGENITAL RETT-SYNDROME PHENOTYPE - DELETION SHORT ARM CHROMOSOME-3, European child & adolescent psychiatry, 6, 1997, pp. 95-95
INTRODUCING FISH INTO PRENATAL-DIAGNOSIS
Authors: VUJIC M ARSIC N SRETENOVIC Z BRANKOVIC S STEVANOVIC M
Citation: M. Vujic et al., INTRODUCING FISH INTO PRENATAL-DIAGNOSIS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 56-56
MATERNAL ORIGIN OF INV DUP(15) CHROMOSOMES IN INFANTILE-AUTISM
Authors: MARTINSSON T JOHANNESSON T VUJIC M SJOSTEDT A STEFFENBURG S GILLBERG C WAHLSTROM J
Citation: T. Martinsson et al., MATERNAL ORIGIN OF INV DUP(15) CHROMOSOMES IN INFANTILE-AUTISM, European child & adolescent psychiatry, 5(4), 1996, pp. 185-192
LOCALIZATION OF A GENE FOR AUTOSOMAL-DOMINANT LARSEN SYNDROME TO CHROMOSOME REGION 3P21.1-14.1 IN THE PROXIMITY OF, BUT DISTINCT FROM, THE COL7A1 LOCUS
Authors: VUJIC M HALLSTENSSON K WAHLSTROM J LUNDBERG A LANGMAACK C MARTINSSON T
Citation: M. Vujic et al., LOCALIZATION OF A GENE FOR AUTOSOMAL-DOMINANT LARSEN SYNDROME TO CHROMOSOME REGION 3P21.1-14.1 IN THE PROXIMITY OF, BUT DISTINCT FROM, THE COL7A1 LOCUS, American journal of human genetics, 57(5), 1995, pp. 1104-1113
LINKAGE OF A GENE FOR AUTOSOMAL-DOMINANT LARSEN SYNDROME (LAR1) TO CHROMOSOME 3P-MARKERS
Authors: MARTINSSON T VUJIC M HALLSTENSSON K LUNDBERG A LANGMAACK C WAHLSTROM J
Citation: T. Martinsson et al., LINKAGE OF A GENE FOR AUTOSOMAL-DOMINANT LARSEN SYNDROME (LAR1) TO CHROMOSOME 3P-MARKERS, American journal of human genetics, 57(4), 1995, pp. 1133-1133
SWEDISH SURVEY ON EXTRA STRUCTURALLY ABNORMAL CHROMOSOMES IN 39105 CONSECUTIVE PRENATAL DIAGNOSES - PREVALENCE AND CHARACTERIZATION BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: BLENNOW E BUI TH KRISTOFFERSSON U VUJIC M ANNEREN G HOLMBERG E NORDENSKJOLD M
Citation: E. Blennow et al., SWEDISH SURVEY ON EXTRA STRUCTURALLY ABNORMAL CHROMOSOMES IN 39105 CONSECUTIVE PRENATAL DIAGNOSES - PREVALENCE AND CHARACTERIZATION BY FLUORESCENCE IN-SITU HYBRIDIZATION, Prenatal diagnosis, 14(11), 1994, pp. 1019-1028
LOCALIZATION OF THE HUMAN TRIPEPTIDYL PEPTIDASE-II GENE (TPP2) TO 13Q32-Q33 BY NONRADIOACTIVE IN-SITU HYBRIDIZATION AND SOMATIC-CELL HYBRIDS
Authors: MARTINSSON T VUJIC M TOMKINSON B
Citation: T. Martinsson et al., LOCALIZATION OF THE HUMAN TRIPEPTIDYL PEPTIDASE-II GENE (TPP2) TO 13Q32-Q33 BY NONRADIOACTIVE IN-SITU HYBRIDIZATION AND SOMATIC-CELL HYBRIDS, Genomics, 17(2), 1993, pp. 493-495
CHROMOSOMAL LOCALIZATION OF THE HUMAN TRIPEPTIDYL PEPTIDASE-II (TPP2)GENE TO 13Q32-33
Authors: MARTINSSON T VUJIC M TOMKINSON B
Citation: T. Martinsson et al., CHROMOSOMAL LOCALIZATION OF THE HUMAN TRIPEPTIDYL PEPTIDASE-II (TPP2)GENE TO 13Q32-33, American journal of human genetics, 53(3), 1993, pp. 1788-1788
Risultati: 1-9 |