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American Journal of Human Genetics|May 12, 2009
The diversity present in 5140 human mitochondrial genomesLuísa Pereira, Fernando Freitas, Verónica Fernandes, et al.American Journal of Human Genetics|March 10, 2009
Genome-wide association and replication studies identified TRHR as an important gene for lean body massXiao-Gang Liu, Li-Jun Tan, Shu-Feng Lei, et al.American Journal of Human Genetics|March 10, 2009
Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosaHui Wang, Anneke I den Hollander, Yalda Moayedi, et al.American Journal of Human Genetics|November 1, 1991
Using medical genetics applications to educate for computer competenceJ A MitchellAmerican Journal of Human Genetics|November 1, 1991
Complex segregation analysis of autismL B Jorde, S J Hasstedt, E R Ritvo, et al.American Journal of Human Genetics|November 1, 1991
Linkage disequilibrium between two highly polymorphic microsatellitesR Sherrington, G Melmer, M Dixon, et al.American Journal of Human Genetics|November 1, 1991
De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpointsD WarburtonAmerican Journal of Human Genetics|June 9, 2009
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformationsPaweł Stankiewicz, Partha Sen, Samarth S Bhatt, et al.American Journal of Human Genetics|May 5, 2009
Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in miceDavid A Parry, Carmel Toomes, Lina Bida, et al.American Journal of Human Genetics|May 5, 2009
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic diseaseDong-Chuan Guo, Christina L Papke, Van Tran-Fadulu, et al.Pageof 979