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American Journal of Human Genetics|April 23, 2013
FOXP2 targets show evidence of positive selection in European populationsQasim Ayub, Bryndis Yngvadottir, Yuan Chen, et al.American Journal of Human Genetics|June 4, 2013
Enhanced localization of genetic samples through linkage-disequilibrium correctionYael Baran, Inés Quintela, Angel Carracedo, et al.American Journal of Human Genetics|May 14, 2013
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegiaEmily C Oates, Alexander M Rossor, Majid Hafezparast, et al.American Journal of Human Genetics|June 18, 2013
General framework for meta-analysis of rare variants in sequencing association studiesSeunggeun Lee, Tanya M Teslovich, Michael Boehnke, et al.American Journal of Human Genetics|April 30, 2013
Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemiaMassimo Bogliolo, Beatrice Schuster, Chantal Stoepker, et al.American Journal of Human Genetics|April 30, 2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticityHiromi Hirata, Indrajit Nanda, Anne van Riesen, et al.American Journal of Human Genetics|April 9, 2013
GIGI: an approach to effective imputation of dense genotypes on large pedigreesCharles Y K Cheung, Elizabeth A Thompson, Ellen M WijsmanAmerican Journal of Human Genetics|April 9, 2013
Improving the accuracy and efficiency of partitioning heritability into the contributions of genomic regionsEmrah Kostem, Eleazar EskinAmerican Journal of Human Genetics|June 11, 2013
Long runs of homozygosity are enriched for deleterious variationZachary A Szpiech, Jishu Xu, Trevor J Pemberton, et al.American Journal of Human Genetics|June 11, 2013
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathyGianina Ravenscroft, Satoko Miyatake, Vilma-Lotta Lehtokari, et al.Pageof 980