AAAAAA

   
Results: 1-7 |
Results: 7
Population genomics: a bridge from evolutionary history to genetic medicine
Authors: Jorde, LB Watkins, WS Bamshad, MJ
Citation: Lb. Jorde et al., Population genomics: a bridge from evolutionary history to genetic medicine, HUM MOL GEN, 10(20), 2001, pp. 2199-2207
Clinical analysis of families with heart, midline, and laterality defects
Authors: Morelli, SH Young, L Reid, B Ruttenberg, H Bamshad, MJ
Citation: Sh. Morelli et al., Clinical analysis of families with heart, midline, and laterality defects, AM J MED G, 101(4), 2001, pp. 388-392
Patterns of ancestral human diversity: An analysis of Alu-insertion and restriction-site polymorphisms
Authors: Watkins, WS Ricker, CE Bamshad, MJ Carroll, ML Nguyen, SV Batzer, MA Harpending, HC Rogers, AR Jorde, LB
Citation: Ws. Watkins et al., Patterns of ancestral human diversity: An analysis of Alu-insertion and restriction-site polymorphisms, AM J HU GEN, 68(3), 2001, pp. 738-752
The distribution of human genetic diversity: A comparison of mitochondrial, autosomal, and Y-chromosome data
Authors: Jorde, LB Watkins, WS Bamshad, MJ Dixon, ME Ricker, CE Seielstad, MT Batzer, MA
Citation: Lb. Jorde et al., The distribution of human genetic diversity: A comparison of mitochondrial, autosomal, and Y-chromosome data, AM J HU GEN, 66(3), 2000, pp. 979-988
Deep common ancestry of Indian and western-Eurasian mitochondrial DNA lineages
Authors: Kivisild, T Bamshad, MJ Kaldma, K Metspalu, M Metspalu, E Reidla, M Laos, S Parik, J Watkins, WS Dixon, ME Papiha, SS Mastana, SS Mir, MR Ferak, V Villems, R
Citation: T. Kivisild et al., Deep common ancestry of Indian and western-Eurasian mitochondrial DNA lineages, CURR BIOL, 9(22), 1999, pp. 1331-1334
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): Phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3
Authors: Bellus, GA Bamshad, MJ Przylepa, KA Dorst, J Lee, RR Hurko, O Jabs, EW Curry, CJR Wilcox, WR Lachman, RS Rimoin, DL Francomano, CA
Citation: Ga. Bellus et al., Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): Phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3, AM J MED G, 85(1), 1999, pp. 53-65
A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene
Authors: Tavormina, PL Bellus, GA Webster, MK Bamshad, MJ Fraley, AE McIntosh, I Szabo, J Jiang, W Jabs, EW Wilcox, WR Wasmuth, JJ Donoghue, DJ Thompson, LM Francomano, CA
Citation: Pl. Tavormina et al., A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene, AM J HU GEN, 64(3), 1999, pp. 722-731
Risultati: 1-7 |