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Genomics|December 1, 1991
Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8S H Blanton, J R Heckenlively, A W Cottingham, et al.Chinese Medical Journal|June 1, 1992
Linkage between Rh blood group and autosomal dominant retinitis pigmentosa in ten Chinese familiesY J Fei, S H Blanton, S P Daiger, et al.Genomics|September 1, 1992
Human chromosome 8 linkage map based on short tandem repeat polymorphisms: effect of genotyping errorsJ Tomfohrde, S Wood, M Schertzer, et al.American Journal of Human Genetics|June 1, 1993
Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13AJ T Hecht, Y Wang, B Connor, et al.American Journal of Human Genetics|September 1, 1991
Cleft lip and palate: no evidence of linkage to transforming growth factor alphaJ T Hecht, Y P Wang, S H Blanton, et al.Genomics|September 1, 1990
Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3qS H Blanton, A W Cottingham, N Giesenschlag, et al.American Journal of Human Genetics|July 1, 1995
X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11R E McGuire, L S Sullivan, S H Blanton, et al.American Journal of Medical Genetics|November 1, 1992
Exclusion of human proteoglycan link protein (CRTL1) and type II collagen (COL2A1) genes in pseudoachondroplasiaJ T Hecht, S H Blanton, Y Wang, et al.Genomics|December 24, 1997
Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24R W Yee, L S Sullivan, H T Lai, et al.American Journal of Medical Genetics|January 1, 1983
Deletion mapping of polymorphic loci by apparent parental exclusionS P Daiger, A ChakravartiPageof 12