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Behavior Genetics|July 1, 1995
Oligogenic determination of morphine analgesic magnitude: a genetic analysis of selectively bred mouse linesJ S Mogil, P Flodman, M A Spence, et al.Biological Psychiatry|November 1, 1995
Evidence for heritability of biogenic amine levels in the cerebrospinal fluid of rhesus monkeysA S Clarke, C M Kammerer, K P George, et al.Ophthalmology|April 1, 1988
Genetic linkage analysis of autosomal dominant congenital cataracts with lens-specific DNA probes and polymorphic phenotypic markersD J Barrett, R S Sparkes, M B Gorin, et al.Genomics|January 1, 1990
Ornithine aminotransferase (OAT): recombination between an X-linked OAT sequence (7.5 kb) and the Norrie disease locusJ T Ngo, J B Bateman, M A Spence, et al.Molecular Psychiatry|March 13, 2001
No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorderS P Hamilton, S L Slager, L Helleby, et al.Ophthalmic Research|January 1, 1982
Possible assignment of a dominant retinitis pigmentosa gene to chromosome 1J R Heckenlively, J T Pearlman, R S Sparkes, et al.Investigative Ophthalmology & Visual Science|September 28, 2000
A new betaA1-crystallin splice junction mutation in autosomal dominant cataractJ B Bateman, D D Geyer, P Flodman, et al.Journal of Craniofacial Genetics and Developmental Biology|January 1, 1983
Genetic linkage studies with cleft lip and palate: report of two family studiesM A Spence, L Glass, B F Crandall, et al.American Journal of Human Genetics|February 1, 1996
Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosaT L Kojis, C Heinzmann, P Flodman, et al.The European Respiratory Journal|October 3, 2002
BMPR2 germline mutations in pulmonary hypertension associated with fenfluramine derivativesM Humbert, Z Deng, G Simonneau, et al.Pageof 19