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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.Molecular Psychiatry|March 28, 2003
Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12J Liu, S H Juo, A Dewan, et al.American Journal of Human Genetics|June 13, 1998
No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigreesJ A Knowles, P A Rao, T Cox-Matise, 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.Pageof 8