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Journal of Medical Genetics|October 1, 1986
Replication status of fragile X(q27.3) in 13 female heterozygotesE Tuckerman, T Webb, A ThakeJournal of Medical Genetics|October 1, 1986
Three children with partial trisomy 1q and partial monosomy 3pG T McCarthy, C N Fear, A C BerryJournal of Medical Genetics|October 1, 1986
Terminal deletion of the long arm of chromosome 10H Curtis, R T Howell, C CopeJournal of Medical Genetics|March 19, 2002
Leber hereditary optic neuropathyP Yu-Wai-Man, D M Turnbull, P F ChinneryJournal of Medical Genetics|March 19, 2002
Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomasB E Baysal, J E Willett-Brozick, E C Lawrence, et al.Journal of Medical Genetics|October 1, 1993
Upper and lower neural tube defects: an alternate hypothesisB H Garabedian, F C FraserJournal of Medical Genetics|October 1, 1993
Orofaciodigital syndrome type III in two sibsR A Smith, D Gardner-MedwinJournal of Medical Genetics|October 1, 1993
Airway abnormalities in Jarcho-Levin syndrome: a report of two casesM Schulman, M T Gonzalez, M R ByeJournal of Medical Genetics|April 1, 1993
Six DNA polymorphisms in the low density lipoprotein receptor gene: their genetic relationship and an example of their use for identifying affected relatives of patients with familial hypercholesterolaemiaS Humphries, L King-Underwood, V Gudnason, et al.Journal of Medical Genetics|June 1, 1993
Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26M A Pericak-Vance, K J Nunes, E Whisenant, et al.Pageof 649