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Annals of Neurology|August 2, 2003
Association between genetic variation of CACNA1H and childhood absence epilepsyYucai Chen, Jianjun Lu, Hong Pan, et al.American Journal of Human Genetics|January 20, 2007
Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndromeXiuli Zhao, Miao Sun, Jin Zhao, et al.Oncogene|December 8, 2004
Tumor suppressive role of a 2.4 Mb 9q33-q34 critical region and DEC1 in esophageal squamous cell carcinomaLichun Yang, Alfred C C Leung, Josephine M Y Ko, et al.Oncogene|June 27, 2006
Identification of a tumor suppressive critical region mapping to 3p14.2 in esophageal squamous cell carcinoma and studies of a candidate tumor suppressor gene, ADAMTS9P H Y Lo, A C C Leung, C Y C Kwok, et al.Journal of Medical Genetics|April 18, 2008
Triphalangeal thumb-polysyndactyly syndrome and syndactyly type IV are caused by genomic duplications involving the long range, limb-specific SHH enhancerM Sun, F Ma, X Zeng, et al.Schizophrenia Research|January 30, 2016
A randomized controlled trial on the psychophysiological effects of physical exercise and Tai-chi in patients with chronic schizophreniaRainbow T H Ho, Ted C T Fong, Adrian H Y Wan, et al.Molecular Cancer Research : MCR|April 12, 2008
Monochromosome transfer and microarray analysis identify a critical tumor-suppressive region mapping to chromosome 13q14 and THSD1 in esophageal carcinomaJosephine M Y Ko, Pui Ling Chan, Wing Lung Yau, et al.American Journal of Human Genetics|May 26, 2009
Copy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasiaMiao Sun, Ning Li, Wu Dong, et al.Nature Genetics|January 6, 2009
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosisYaran Wen, Yang Liu, Yiming Xu, et al.Pageof 9