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Nature Genetics|April 16, 2002
Segregation at three loci explains familial and population risk in Hirschsprung diseaseStacey B Gabriel, Rémi Salomon, Anna Pelet, et al.
Plos Genetics|April 19, 2012
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autismMaria H Chahrour, Timothy W Yu, Elaine T Lim, et al.
Early Intervention in Psychiatry|July 17, 2015
Domain-specific impairment in cognitive control among remitted youth with a history of major depressionAmy T Peters, Rachel H Jacobs, Natania A Crane, et al.
Human Molecular Genetics|January 8, 2011
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13Minal Çalışkan, Jessica X Chong, Lawrence Uricchio, et al.
Cell Reports|June 30, 2015
Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi AnemiaKimberly A Rickman, Francis P Lach, Avinash Abhyankar, et al.
Nature Genetics|July 19, 2016
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discoveryEric M Scott, Anason Halees, Yuval Itan, et al.
Brain : a Journal of Neurology|March 31, 2015
Shared dimensions of performance and activation dysfunction in cognitive control in females with mood disordersKelly A Ryan, Erica L Dawson, Michelle T Kassel, et al.
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