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
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
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
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
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