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American Journal of Human Genetics|May 19, 2004
Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type ILChristian G Frank, Claudia E Grubenmann, Wafaa Eyaid, et al.American Journal of Human Genetics|April 3, 2004
Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic IsolatesRonald G Lafreniere, Marcia L E MacDonald, Marie-Pierre Dube, et al.American Journal of Human Genetics|April 6, 2004
Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22Linda M Brzustowicz, Jaime Simone, Paria Mohseni, et al.American Journal of Human Genetics|May 5, 2004
Mutations of the ephrin-B1 gene cause craniofrontonasal syndromeIlse Wieland, Sibylle Jakubiczka, Petra Muschke, et al.American Journal of Human Genetics|January 20, 2004
Genomewide linkage analysis for internal carotid artery intimal medial thickness: evidence for linkage to chromosome 12Caroline S Fox, L Adrienne Cupples, Irmarie Chazaro, et al.American Journal of Human Genetics|January 24, 2004
Null leukemia inhibitory factor receptor (LIFR) mutations in Stuve-Wiedemann/Schwartz-Jampel type 2 syndromeNathalie Dagoneau, Deborah Scheffer, Céline Huber, et al.American Journal of Human Genetics|January 21, 2004
Inherent bias toward the null hypothesis in conventional multipoint nonparametric linkage analysisNicholas J Schork, Tiffany A GreenwoodAmerican Journal of Human Genetics|December 19, 2003
Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defectsStephanie M Ware, Jianlan Peng, Lirong Zhu, et al.American Journal of Human Genetics|December 19, 2003
The burden of genetic disease on inpatient care in a children's hospitalShawn E McCandless, Jeanne W Brunger, Suzanne B CassidyAmerican Journal of Human Genetics|December 20, 2003
Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benignJoshua D Groman, Timothy W Hefferon, Teresa Casals, et al.Pageof 979