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Journal of Human Genetics|January 23, 2009
Identification of novel EIF2B mutations in Chinese patients with vanishing white matter diseaseYe Wu, Yanxia Pan, Li Du, et al.
Journal of Human Genetics|January 23, 2009
Genetic correlation between autistic traits and IQ in a population-based sample of twins with autism spectrum disorders (ASDs)Takeshi Nishiyama, Hiroko Taniai, Hitomi Taniai, et al.
Journal of Human Genetics|January 23, 2009
Two-stage case-control association study of polymorphisms in rheumatoid arthritis susceptibility genes with schizophreniaYuichiro Watanabe, Ayako Nunokawa, Naoshi Kaneko, et al.
Journal of Human Genetics|January 23, 2009
Identification of multidrug and toxin extrusion (MATE1 and MATE2-K) variants with complete loss of transport activityMoto Kajiwara, Tomohiro Terada, Ken Ogasawara, et al.
Journal of Human Genetics|August 13, 2010
Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhageJoon Seol Bae, Hyun Sub Cheong, Byung Lae Park, et al.
Journal of Human Genetics|November 19, 2010
SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean populationJong-Min Kim, Sue K Park, Jae Jeong Yang, et al.
Journal of Human Genetics|February 11, 2011
Association of the arginine vasopressin receptor 1A (AVPR1A) haplotypes with listening to musicLiisa Ukkola-Vuoti, Jaana Oikkonen, Päivi Onkamo, et al.
Journal of Human Genetics|February 11, 2011
Clinical and molecular genetic analysis in Chinese patients with distal myopathy with rimmed vacuolesHonghao Li, Qi Chen, Fuchen Liu, et al.
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