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American Journal of Human Genetics|March 16, 2007
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphismsStacey Melquist, David W Craig, Matthew J Huentelman, et al.American Journal of Human Genetics|March 16, 2007
Medical sequencing at the extremes of human body massNadav Ahituv, Nihan Kavaslar, Wendy Schackwitz, et al.American Journal of Human Genetics|October 13, 2006
Molecular population genetics of the gene encoding the human fertilization protein zonadhesin reveals rapid adaptive evolutionJoe Gasper, Willie J SwansonAmerican Journal of Human Genetics|October 13, 2006
Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigreesEllen M Wijsman, Joseph H Rothstein, Elizabeth A ThompsonAmerican Journal of Human Genetics|October 13, 2006
Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophreniaMousumi Mutsuddi, Derek W Morris, Skye G Waggoner, et al.American Journal of Human Genetics|October 13, 2006
Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypesMarcus G Pezzolesi, Yan Li, Xiao-Ping Zhou, et al.American Journal of Human Genetics|October 13, 2006
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaLars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, et al.American Journal of Human Genetics|December 23, 2006
Powerful multilocus tests of genetic association in the presence of gene-gene and gene-environment interactionsNilanjan Chatterjee, Zeynep Kalaylioglu, Roxana Moslehi, et al.American Journal of Human Genetics|December 23, 2006
Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type IIISven Cichon, Ludovic Martin, Hans Christian Hennies, et al.American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.Pageof 979