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Science (New York, N.Y.)|November 13, 1987
A DNA segment encoding two genes very tightly linked to Huntington's diseaseT C Gilliam, M Bucan, M E MacDonald, et al.
Genomics|September 1, 1987
A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease geneM E MacDonald, M A Anderson, T C Gilliam, et al.
Nature Genetics|December 1, 1992
Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13qK Ben Othmane, M Ben Hamida, M A Pericak-Vance, et al.
American Journal of Medical Genetics|April 17, 2001
A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22J Liu, S H Juo, J D Terwilliger, et al.
Investigative Ophthalmology & Visual Science|August 10, 1999
Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degenerationC A Lewis, I R Batlle, K G Batlle, et al.
Nature Genetics|February 14, 1998
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosaP Banerjee, P W Kleyn, J A Knowles, et al.
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