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American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, et al.Journal of Medical Genetics|June 17, 2005
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12D Yan, X Ke, S H Blanton, et al.American Journal of Human Genetics|January 1, 1997
Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignanciesJ T Hecht, D Hogue, Y Wang, et al.American Journal of Medical Genetics|November 14, 2000
Methylenetetrahydrofolate reductase and spina bifida: evaluation of level of defect and maternal genotypic risk in HispanicsK A Volcik, S H Blanton, G H Tyerman, et al.Genomics|December 1, 1993
Linkage of typical pseudoachondroplasia to chromosome 19J T Hecht, C A Francomano, M D Briggs, et al.American Journal of Human Genetics|August 1, 1995
Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational familiesJ Stein, J B Mulliken, S Stal, et al.American Journal of Human Genetics|July 1, 1993
Genetic heterogeneity in families with hereditary multiple exostosesA Cook, W Raskind, S H Blanton, et al.Human Molecular Genetics|December 10, 1999
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing lossX Z Liu, X J Xia, L R Xu, et al.Genomics|June 15, 1996
Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPOA J Griffith, D L Burgess, D C Kohrman, et al.Journal of Medical Genetics|February 1, 1990
An exclusion map of Marfan syndromeS H Blanton, M Sarfarazi, H Eiberg, et al.Pageof 12