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Results: 1-8 |
Results: 8
MUTATIONS IN HUMAN TBX5 CAUSE LIMB AND CARDIAC MALFORMATION IN HOLT-ORAM-SYNDROME (VOL 15, PG 30, 1997)
Authors: BASSON CT BACHINSKY DR LIN RC LEVI T ELKINS JA SOULTS J GRAYZEL D KROUMPOUZOU E TRAILL TA LEBLANCSTRACESKI J RENAULT B KUCHERLAPATI R SEIDMAN JG SEIDMAN CE
Citation: Ct. Basson et al., MUTATIONS IN HUMAN TBX5 CAUSE LIMB AND CARDIAC MALFORMATION IN HOLT-ORAM-SYNDROME (VOL 15, PG 30, 1997), Nature genetics, 15(4), 1997, pp. 411-411
MUTATIONS IN HUMAN CAUSE LIMB AND CARDIAC MALFORMATION IN HOLT-ORAM SYNDROME
Authors: BASSON CT BACHINSKY DR LIN RC LEVI T ELKINS JA SOULTS J GRAYZEL D KROUMPOUZOU E TRAILL TA LEBLANCSTRACESKI J RENAULT B KUCHERLAPATI R SEIDMAN JG SEIDMAN CE
Citation: Ct. Basson et al., MUTATIONS IN HUMAN CAUSE LIMB AND CARDIAC MALFORMATION IN HOLT-ORAM SYNDROME, Nature genetics, 15(1), 1997, pp. 30-35
ASSIGNMENT OF THE HUMAN MYOGENIC FACTOR-5 AND FACTOR-6 (MYF5, MYF6) GENE-CLUSTER TO 12Q21 BY IN-SITU HYBRIDIZATION AND PHYSICAL MAPPING OF THE LOCUS BETWEEN D12S350 AND D12S106
Authors: CUPELLI L RENAULT B LEBLANCSTRACESKI J BANKS A WARD D KUCHERLAPATI RS KRAUTER K
Citation: L. Cupelli et al., ASSIGNMENT OF THE HUMAN MYOGENIC FACTOR-5 AND FACTOR-6 (MYF5, MYF6) GENE-CLUSTER TO 12Q21 BY IN-SITU HYBRIDIZATION AND PHYSICAL MAPPING OF THE LOCUS BETWEEN D12S350 AND D12S106, Cytogenetics and cell genetics, 72(2-3), 1996, pp. 250-251
A 2ND-GENERATION YAC CONTIG MAP OF HUMAN-CHROMOSOME-12
Authors: KRAUTER K MONTGOMERY K YOON SJ LEBLANCSTRACESKI J RENAULT B MARONDEL I HERDMAN V CUPELLI L BANKS A LIEMAN J MENNINGER J BRAYWARD P NADKARNI P WEISSENBACH J LEPASLIER D RIGAULT P CHUMAKOV I COHEN D MILLER P WARD D KUCHERLAPATI R
Citation: K. Krauter et al., A 2ND-GENERATION YAC CONTIG MAP OF HUMAN-CHROMOSOME-12, Nature, 377, 1995, pp. 321-333
ORGANIZATION OF THE HUMAN KERATIN TYPE-II GENE-CLUSTER AT 12Q13
Authors: YOON SJ LEBLANCSTRACESKI J WARD D KRAUTER K KUCHERLAPATI R
Citation: Sj. Yoon et al., ORGANIZATION OF THE HUMAN KERATIN TYPE-II GENE-CLUSTER AT 12Q13, Genomics, 24(3), 1994, pp. 502-508
LINKAGE ANALYSES IN BRITISH PEDIGREES SUGGEST A SINGLE-LOCUS FOR DARIER DISEASE AND NARROW THE LOCATION TO THE INTERVAL BETWEEN D12S105 ANDD12S129
Authors: CARTER SA BRYCE SD MUNRO CS HEALY E BASHIR R WEISSENBACH J LEBLANCSTRACESKI J KUCHERLAPATI R STEPHENSON A REES JL STRACHAN T
Citation: Sa. Carter et al., LINKAGE ANALYSES IN BRITISH PEDIGREES SUGGEST A SINGLE-LOCUS FOR DARIER DISEASE AND NARROW THE LOCATION TO THE INTERVAL BETWEEN D12S105 ANDD12S129, Genomics, 24(2), 1994, pp. 378-382
MOLECULAR MAPPING OF 12Q22 DELETIONS IN MALE GERM-CELL TUMORS
Authors: MURTY VVVS BOSL G LEBLANCSTRACESKI J KUCHERLAPATI R CHAGANTI RSK
Citation: Vvvs. Murty et al., MOLECULAR MAPPING OF 12Q22 DELETIONS IN MALE GERM-CELL TUMORS, Cytogenetics and cell genetics, 67(4), 1994, pp. 271-272
MUTATIONS IN THE NON-HELICAL LINKER SEGMENT L1-2 OF KERATIN-5 IN PATIENTS WITH WEBER-COCKAYNE EPIDERMOLYSIS-BULLOSA SIMPLEX
Authors: CHAN YM YU QC LEBLANCSTRACESKI J CHRISTIANO A PULKKINEN L KUCHERLAPATI RS UITTO J FUCHS E
Citation: Ym. Chan et al., MUTATIONS IN THE NON-HELICAL LINKER SEGMENT L1-2 OF KERATIN-5 IN PATIENTS WITH WEBER-COCKAYNE EPIDERMOLYSIS-BULLOSA SIMPLEX, Journal of Cell Science, 107, 1994, pp. 765-774
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