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Results: 1-25 | 26-29
Results: 1-25/29
ANALYSIS OF MICROTUBULE-ASSOCIATED PROTEIN 1A GENE IN HEREDITARY SPASTIC PARAPLEGIA
Authors: RAINIER S JONES SM ESPOSITO C GUICE E OTTERUD B LEPPERT M FINK JK
Citation: S. Rainier et al., ANALYSIS OF MICROTUBULE-ASSOCIATED PROTEIN 1A GENE IN HEREDITARY SPASTIC PARAPLEGIA, Neurology, 51(5), 1998, pp. 1509-1510
GENETIC-MAPPING OF OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF THE SPINE
Authors: KOGA H SAKOU T TAKETOMI E HAYASHI K NUMASAWA T HARATA S YONE K MATSUNAGA S OTTERUD B INOUE I LEPPERT M
Citation: H. Koga et al., GENETIC-MAPPING OF OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF THE SPINE, American journal of human genetics, 62(6), 1998, pp. 1460-1467
MUTATIONS IN CYP1B1, THE GENE FOR CYTOCHROME P4501B1, ARE THE PREDOMINANT CAUSE OF PRIMARY CONGENITAL GLAUCOMA IN SAUDI-ARABIA
Authors: BEJJANI BA LEWIS RA TOMEY KF ANDERSON KL DUEKER DK JABAK M ASTLE WF OTTERUD B LEPPERT M LUPSKI JR
Citation: Ba. Bejjani et al., MUTATIONS IN CYP1B1, THE GENE FOR CYTOCHROME P4501B1, ARE THE PREDOMINANT CAUSE OF PRIMARY CONGENITAL GLAUCOMA IN SAUDI-ARABIA, American journal of human genetics, 62(2), 1998, pp. 325-333
A FAMILIAL PLATELET DISORDER WITH PROPENSITY TO DEVELOP ACUTE MYELOID-LEUKEMIA IS LINKED TO HUMAN-CHROMOSOME 21Q22.1-Q22.2
Authors: LEGARE RD HO CY OTTERUD B VARVIL T SAXENA R GALLAGHER M LU D DEHART D KOHLER S LI F LEPPERT M GILLILAND DG
Citation: Rd. Legare et al., A FAMILIAL PLATELET DISORDER WITH PROPENSITY TO DEVELOP ACUTE MYELOID-LEUKEMIA IS LINKED TO HUMAN-CHROMOSOME 21Q22.1-Q22.2, Cytogenetics and cell genetics, 79(1-2), 1997, pp. 51-52
MUTATIONS IN CYTOCHROME P450B1 (CYP1B1) AS THE MAIN CAUSE OF PRIMARY CONGENITAL GLAUCOMA (PCG) IN SAUDI-ARABIA AND ECUADOR
Authors: BEJJANI BA LEWIS RA ANDERSON KL TOMEY KF ASTLE WF DUEKER DK MOLINARI A OTTERUD B LEPPERT M LUPSKI JR
Citation: Ba. Bejjani et al., MUTATIONS IN CYTOCHROME P450B1 (CYP1B1) AS THE MAIN CAUSE OF PRIMARY CONGENITAL GLAUCOMA (PCG) IN SAUDI-ARABIA AND ECUADOR, American journal of human genetics, 61(4), 1997, pp. 1907-1907
A GENE FOR PRIMARY CONGENITAL GLAUCOMA IS NOT LINKED TO THE LOCUS ON CHROMOSOME 1Q FOR AUTOSOMAL-DOMINANT JUVENILE-ONSET OPEN-ANGLE GLAUCOMA
Authors: ANDERSON KL LEWIS RA BEJJANI BA BAIRD L OTTERUD B TOMEY KF ASTLE WF DUEKER DK LEPPERT M LUPSKI JR
Citation: Kl. Anderson et al., A GENE FOR PRIMARY CONGENITAL GLAUCOMA IS NOT LINKED TO THE LOCUS ON CHROMOSOME 1Q FOR AUTOSOMAL-DOMINANT JUVENILE-ONSET OPEN-ANGLE GLAUCOMA, Journal of glaucoma, 5(6), 1996, pp. 416-421
DISCORDANCE OF THE MYELIN BASIC-PROTEIN GENE IN FAMILIAL MULTIPLE-SCLEROSIS
Authors: ROSE JW GERKEN S LYNCH S PISANI P HILL K OTTERUD B LEPPERT M
Citation: Jw. Rose et al., DISCORDANCE OF THE MYELIN BASIC-PROTEIN GENE IN FAMILIAL MULTIPLE-SCLEROSIS, Annals of neurology, 40(3), 1996, pp. 118-118
LOCALIZATION OF GENES ENCODING 2 HLA-B7 RESTRICTED MINOR HISTOCOMPATIBILITY ANTIGENS TO CHROMOSOME-22 AND CHROMOSOME-11
Authors: BEATTY PG GUBAREV M JENKIN J LEPPERT M OTTERUD B BUCHANAN G
Citation: Pg. Beatty et al., LOCALIZATION OF GENES ENCODING 2 HLA-B7 RESTRICTED MINOR HISTOCOMPATIBILITY ANTIGENS TO CHROMOSOME-22 AND CHROMOSOME-11, Human immunology, 49, 1996, pp. 37-37
HEREDITARY SPASTIC PARAPLEGIA LINKED TO CHROMOSOME 15Q - ANALYSIS OF CANDIDATE GENES
Authors: FINK JK JONES SM SHARP GB LANGE BM OTTERUD B LEPPERT M
Citation: Jk. Fink et al., HEREDITARY SPASTIC PARAPLEGIA LINKED TO CHROMOSOME 15Q - ANALYSIS OF CANDIDATE GENES, Neurology, 46(3), 1996, pp. 835-836
AUTOSOMAL-DOMINANT SPINOCEREBELLAR ATAXIA WITH SENSORY AXONAL NEUROPATHY (SCA4) - CLINICAL DESCRIPTION AND GENETIC LOCALIZATION TO CHROMOSOME 16Q22.1
Authors: FLANIGAN K GARDNER K ALDERSON K GALSTER B OTTERUD B LEPPERT MF KAPLAN C PTACEK LJ
Citation: K. Flanigan et al., AUTOSOMAL-DOMINANT SPINOCEREBELLAR ATAXIA WITH SENSORY AXONAL NEUROPATHY (SCA4) - CLINICAL DESCRIPTION AND GENETIC LOCALIZATION TO CHROMOSOME 16Q22.1, American journal of human genetics, 59(2), 1996, pp. 392-399
PAROXYSMAL DYSTONIC CHOREOATHETOSIS - TIGHT LINKAGE TO CHROMOSOME 2Q
Authors: FINK JK RAINIER S WILKOWSKI J JONES SM KUME A HEDERA P ALBIN R MATHAY J GIRBACH L VARVIL T OTTERUD B LEPPERT M
Citation: Jk. Fink et al., PAROXYSMAL DYSTONIC CHOREOATHETOSIS - TIGHT LINKAGE TO CHROMOSOME 2Q, American journal of human genetics, 59(1), 1996, pp. 140-145
GENETIC-MAPPING OF ADRENERGIC-RECEPTOR GENES IN HUMANS
Authors: HOEHE MR OTTERUD B HSIEH WT MARTINEZ MM STAUFFER D HOLIK J BERRETTINI WH BYERLEY WF GERSHON ES LALOUEL JM LEPPERT M
Citation: Mr. Hoehe et al., GENETIC-MAPPING OF ADRENERGIC-RECEPTOR GENES IN HUMANS, Journal of molecular medicine, 73(6), 1995, pp. 299-306
LINKAGE OF FAMILIAL SPASTIC PARAPLEGIA TO CHROMOSOME-15Q - PHENOTYPE GENOTYPE CORRELATIONS/
Authors: FINK JK JONES SM WU CTB SHARP GB LANGE B OTTERUD B LEPPERT M
Citation: Jk. Fink et al., LINKAGE OF FAMILIAL SPASTIC PARAPLEGIA TO CHROMOSOME-15Q - PHENOTYPE GENOTYPE CORRELATIONS/, Journal of cellular biochemistry, 1995, pp. 97-97
FAMILIAL SPASTIC PARAPLEGIA LINKED TO CHROMOSOME-15Q - ANALYSIS OF CANDIDATE GENES
Authors: FINK JK JONES SM WU CT SHARP GB LANGE B OTTERUD B LEPPERT M
Citation: Jk. Fink et al., FAMILIAL SPASTIC PARAPLEGIA LINKED TO CHROMOSOME-15Q - ANALYSIS OF CANDIDATE GENES, Neurology, 45(4), 1995, pp. 439-439
AUTOSOMAL-DOMINANT, FAMILIAL SPASTIC PARAPLEGIA, TYPE-I - CLINICAL AND GENETIC-ANALYSIS OF A LARGE NORTH-AMERICAN FAMILY
Authors: FINK JK SHARP GB LANGE BM WU CB HALEY T OTTERUD B PEACOCK M LEPPERT M
Citation: Jk. Fink et al., AUTOSOMAL-DOMINANT, FAMILIAL SPASTIC PARAPLEGIA, TYPE-I - CLINICAL AND GENETIC-ANALYSIS OF A LARGE NORTH-AMERICAN FAMILY, Neurology, 45(2), 1995, pp. 325-331
A FAMILIAL PLATELET DISORDER WITH PROPENSITY TO DEVELOP ACUTE MYELOID-LEUKEMIA IS LINKED TO HUMAN-CHROMOSOME 21Q22.1-22.2
Authors: LEGARE RD HO CY OTTERUD B VARVIL T GALLAGHER M LI F LEPPERT M GILLILAND DG
Citation: Rd. Legare et al., A FAMILIAL PLATELET DISORDER WITH PROPENSITY TO DEVELOP ACUTE MYELOID-LEUKEMIA IS LINKED TO HUMAN-CHROMOSOME 21Q22.1-22.2, Blood, 86(10), 1995, pp. 3056-3056
A YAC CONTIG ENCOMPASSING THE RECESSIVE STARGARDT DISEASE GENE (STGD)ON CHROMOSOME 1P
Authors: ANDERSON KL BAIRD L LEWIS RA CHINAULT AC OTTERUD B LEPPERT M LUPSKI JR
Citation: Kl. Anderson et al., A YAC CONTIG ENCOMPASSING THE RECESSIVE STARGARDT DISEASE GENE (STGD)ON CHROMOSOME 1P, American journal of human genetics, 57(6), 1995, pp. 1351-1363
A FAMILIAL PLATELET DISORDER WITH PROPENSITY TO DEVELOP ACUTE MYELOID-LEUKEMIA IS LINKED TO HUMAN-CHROMOSOME 21Q22.1-22.2
Authors: LEGARE RD HO CY OTTERUD B VARVIL T SAXENA R GALLAGHER M DEHART D KOHLER S LI F LEPPERT M GILLILAND DG
Citation: Rd. Legare et al., A FAMILIAL PLATELET DISORDER WITH PROPENSITY TO DEVELOP ACUTE MYELOID-LEUKEMIA IS LINKED TO HUMAN-CHROMOSOME 21Q22.1-22.2, American journal of human genetics, 57(4), 1995, pp. 109-109
A YAC CONTIG ENCOMPASSING THE RECESSIVE STARGARDTS-DISEASE GENE STGD ON CHROMOSOME 1P
Authors: ANDERSON KL BAIRD L LEWIS RA OTTERUD B CHINAULT AC LUPSKI JR LEPPERT M
Citation: Kl. Anderson et al., A YAC CONTIG ENCOMPASSING THE RECESSIVE STARGARDTS-DISEASE GENE STGD ON CHROMOSOME 1P, American journal of human genetics, 57(4), 1995, pp. 1483-1483
A GENE FOR FAMILIAL TOTAL ANOMALOUS PULMONARY VENOUS RETURN MAPS TO CHROMOSOME 4P13-Q12
Authors: BLEYL S NELSON L ODELBERG SJ RUTTENBERG HD OTTERUD B LEPPERT M WARD K
Citation: S. Bleyl et al., A GENE FOR FAMILIAL TOTAL ANOMALOUS PULMONARY VENOUS RETURN MAPS TO CHROMOSOME 4P13-Q12, American journal of human genetics, 56(2), 1995, pp. 408-415
AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA - TIGHT LINKAGE TO CHROMOSOME 15Q
Authors: FINK JK WU CTB JONES SM SHARP GB LANGE BM LESICKI A REINGLASS T VARVIL T OTTERUD B LEPPERT M
Citation: Jk. Fink et al., AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA - TIGHT LINKAGE TO CHROMOSOME 15Q, American journal of human genetics, 56(1), 1995, pp. 188-192
BARDET-BIEDL SYNDROME IS LINKED TO DNA MARKERS ON CHROMOSOME 11Q AND IS GENETICALLY HETEROGENEOUS
Authors: LEPPERT M BAIRD L ANDERSON KL OTTERUD B LUPSKI JR LEWIS RA
Citation: M. Leppert et al., BARDET-BIEDL SYNDROME IS LINKED TO DNA MARKERS ON CHROMOSOME 11Q AND IS GENETICALLY HETEROGENEOUS, Nature genetics, 7(1), 1994, pp. 108-112
DESCRIPTION OF A 2ND MICROSATELLITE MARKER AND LINKAGE ANALYSIS OF THE MUSCLE GLYCOGEN-SYNTHASE LOCUS IN FAMILIAL NIDDM
Authors: ELBEIN SC HOFFMAN M RIDINGER D OTTERUD B LEPPERT M
Citation: Sc. Elbein et al., DESCRIPTION OF A 2ND MICROSATELLITE MARKER AND LINKAGE ANALYSIS OF THE MUSCLE GLYCOGEN-SYNTHASE LOCUS IN FAMILIAL NIDDM, Diabetes, 43(8), 1994, pp. 1061-1065
A FAMILIAL PLATELET DISORDER WITH PROPENSITY TO DEVELOP ACUTE MYELOID-LEUKEMIA IS LINKED TO HUMAN-CHROMOSOME 21Q22.1-22.2
Authors: HO CY OTTERUD B VARVIL T SAXENA R DEHART D KOHLER S LI F LEPPERT M GILLILAND DG
Citation: Cy. Ho et al., A FAMILIAL PLATELET DISORDER WITH PROPENSITY TO DEVELOP ACUTE MYELOID-LEUKEMIA IS LINKED TO HUMAN-CHROMOSOME 21Q22.1-22.2, Blood, 84(10), 1994, pp. 10000318-10000318
A GENE FOR DISTAL ARTHROGRYPOSIS TYPE-I MAPS TO THE PERICENTROMERIC REGION OF CHROMOSOME-9
Authors: BAMSHAD M WATKINS WS ZENGER RK BOHNSACK JF CAREY JC OTTERUD B KRAKOWIAK PA ROBERTSON M JORDE LB
Citation: M. Bamshad et al., A GENE FOR DISTAL ARTHROGRYPOSIS TYPE-I MAPS TO THE PERICENTROMERIC REGION OF CHROMOSOME-9, American journal of human genetics, 55(6), 1994, pp. 1153-1158
Risultati: 1-25 | 26-29