Showing results (81-90 of 3,503) with videos related to
Sort By:
Pageof 351
Journal of Human Genetics|October 19, 2006
Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and TurkeyYoriko Endo, Asako Horinishi, Matthias Vorgerd, et al.Journal of Human Genetics|December 6, 2006
Patients with primary cataract as a genetic pool of DMPK protomutationIgor Medica, Natasa Teran, Marija Volk, et al.Journal of Human Genetics|August 10, 2007
Entropy-based joint analysis for two-stage genome-wide association studiesGuolian Kang, Yijun ZuoJournal of Human Genetics|July 20, 2007
Longevity-associated mitochondrial DNA 5178 C/A polymorphism and its interaction with cigarette consumption are associated with pulmonary function in middle-aged Japanese menAkatsuki Kokaze, Mamoru Ishikawa, Naomi Matsunaga, et al.Journal of Human Genetics|August 29, 2006
Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in TunisiaR El Kares, M R Barbouche, H Elloumi-Zghal, et al.Journal of Human Genetics|September 15, 2006
Association of estrogen receptor alpha gene polymorphisms and lifestyle factors with calcaneal quantitative ultrasound and osteoporosis in postmenopausal Vietnamese womenTran Quang Binh, Toshikatsu Shinka, Nguyen Cong Khan, et al.Journal of Human Genetics|July 13, 2006
Cataracts, ataxia, short stature, and mental retardation in a Chinese family mapped to Xpter-q13.1Xiangming Guo, Huangxuan Shen, Xueshan Xiao, et al.Journal of Human Genetics|July 13, 2006
Identification of novel RMRP mutations and specific founder haplotypes in Japanese patients with cartilage-hair hypoplasiaYuichiro Hirose, Eiji Nakashima, Hirofumi Ohashi, et al.Journal of Human Genetics|July 22, 2006
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotypeMaria do Carmo Costa, Andreia Teixeira-Castro, Marco Constante, et al.Journal of Human Genetics|August 10, 2006
Frequent DAP kinase but not p14 or Apaf-1 hypermethylation in B-cell chronic lymphocytic leukemiaC S Chim, T K Fung, K F Wong, et al.Pageof 351