Genetic variation in South Indian castes: evidence from Y-chromosome, mitochondrial, and autosomal polymorphisms von Watkins, W S, Thara, R, Mowry, B J, Zhang, Y, Witherspoon, D J, Tolpinrud, W, Bamshad, M J, Tirupati, S, Padmavati, R, Smith, H, Nancarrow, D, Filippich, C, Jorde, L B

Volltext

Nonsense mutations of the  -spectrin gene in hereditary pyropoikilocytosis von Tolpinrud, W., Maksimova, Y. D., Forget, B. G., Gallagher, P. G.

Volltext

HapMap tagSNP transferability in multiple populations: General guidelines von Xing, Jinchuan, Witherspoon, David J., Watkins, W. Scott, Zhang, Yuhua, Tolpinrud, Whitney, Jorde, Lynn B.

Volltext

Alu repeats increase local recombination rates von Witherspoon, David J, Watkins, W Scott, Zhang, Yuhua, Xing, Jinchuan, Tolpinrud, Whitney L, Hedges, Dale J, Batzer, Mark A, Jorde, Lynn B

Volltext

Genotype–phenotype analysis of angiotensinogen polymorphisms and essential hypertension: the importance of haplotypes von Watkins, W Scott, Hunt, Steven C, Williams, Gordon H, Tolpinrud, Whitney, Jeunemaitre, Xavier, Lalouel, Jean-Marc, Jorde, Lynn B

Volltext

Genotype―phenotype analysis of angiotensinogen polymorphisms and essential hypertension: the importance of haplotypes von WATKINS, W. Scott, HUNT, Steven C, WILLIAMS, Gordon H, TOLPINRUD, Whitney, JEUNEMAITRE, Xavier, LALOUEL, Jean-Marc, JORDE, Lynn B

Volltext

Identification and Characterization of α-Spectrin Mutations Associated with Inherited Hemolytic Anemia von Tolpinrud, Whitney, Gaetani, Massimiliano, Maksimova, Yelena, Mootien, Sara, Harper, Sandra, Forget, Bernard G., Speicher, David W., Gallagher, Patrick G.

Volltext