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American Journal of Human Genetics|July 25, 2000
Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II geneZ Deng, J H Morse, S L Slager, 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.
Gene|January 13, 1998
Identification of a novel member of the TGF-beta superfamily highly expressed in human placentaL N Lawton, M F Bonaldo, P C Jelenc, et al.
American Journal of Human Genetics|January 23, 1999
A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locusV M Aita, J Liu, J A Knowles, et al.
American Journal of Human Genetics|November 21, 2001
Chromosome-12 mapping of late-onset Alzheimer disease among Caribbean HispanicsR Mayeux, J H Lee, S N Romas, et al.
Journal of Affective Disorders|June 28, 2001
Association between a catechol-o-methyltransferase polymorphism and obsessive-compulsive disorder in the Afrikaner populationD J Niehaus, C J Kinnear, V A Corfield, et al.
Molecular Psychiatry|July 9, 2004
Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean HispanicsJ H Lee, R Mayeux, D Mayo, et al.
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