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American Journal of Human Genetics|September 16, 1999
Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: evidence for a locus on 2qJ Leppävuori, U Kujala, J Kinnunen, et al.American Journal of Human Genetics|September 16, 1999
A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33S Baulac, I Gourfinkel-An, F Picard, et al.American Journal of Human Genetics|September 16, 1999
A novel syndrome of episodic muscle weakness maps to xp22.3M M Ryan, P Taylor, J A Donald, et al.American Journal of Human Genetics|September 16, 1999
A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility lociI Hovatta, T Varilo, J Suvisaari, et al.American Journal of Human Genetics|October 16, 1999
Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasiaI Quack, B Vonderstrass, M Stock, et al.American Journal of Human Genetics|October 16, 1999
High frequency of large intragenic deletions in the Fanconi anemia group A geneN V Morgan, A J Tipping, H Joenje, et al.American Journal of Human Genetics|October 16, 1999
Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancersN Sévenet, E Sheridan, D Amram, et al.American Journal of Human Genetics|October 16, 1999
Hypomethylation of an expanded FMR1 allele is not associated with a global DNA methylation defectR W Burman, P A Yates, L D Green, et al.American Journal of Human Genetics|October 16, 1999
A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome. The Tourette Syndrome Association International Consortium for GeneticsAmerican Journal of Human Genetics|January 13, 2000
Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndromeD Monk, E L Wakeling, V Proud, et al.Pageof 979