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S H Blanton

Showing results (11-20 of 53) with videos related to

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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.
Genetic Testing|January 1, 1997
Implications of molecular diagnostic testing in families with hereditary pancreatitisA Pandya, X J Xia, S H Blanton, et al.
American Journal of Human Genetics|May 1, 1995
Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8J T Hecht, D Hogue, L C Strong, 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.
Genomics|December 1, 1996
Linkage studies in a large kindred with hereditary pancreatitis confirms mapping of the gene to a 16-cM region on 7qA Pandya, S H Blanton, B Landa, et al.
American Journal of Human Genetics|March 1, 1995
Genetic heterogeneity in multiple epiphyseal dysplasiaM Deere, S H Blanton, C I Scott, et al.
Neuropediatrics|April 1, 1996
Cobblestone lissencephaly with normal eyes and muscleW B Dobyns, M A Patton, R F Stratton, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|October 1, 1991
Familial renal adysplasiaB Murugasu, B R Cole, E P Hawkins, 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.
Journal of Medical Genetics|February 11, 1990
Linkage analysis in Marfan syndromeR C Schwartz, S H Blanton, C A Hyde, et al.
Pageof 6

Showing results (11-20 of 53) with videos related to

Sort By:
Pageof 6
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.
Genetic Testing|January 1, 1997
Implications of molecular diagnostic testing in families with hereditary pancreatitisA Pandya, X J Xia, S H Blanton, et al.
American Journal of Human Genetics|May 1, 1995
Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8J T Hecht, D Hogue, L C Strong, 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.
Genomics|December 1, 1996
Linkage studies in a large kindred with hereditary pancreatitis confirms mapping of the gene to a 16-cM region on 7qA Pandya, S H Blanton, B Landa, et al.
American Journal of Human Genetics|March 1, 1995
Genetic heterogeneity in multiple epiphyseal dysplasiaM Deere, S H Blanton, C I Scott, et al.
Neuropediatrics|April 1, 1996
Cobblestone lissencephaly with normal eyes and muscleW B Dobyns, M A Patton, R F Stratton, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|October 1, 1991
Familial renal adysplasiaB Murugasu, B R Cole, E P Hawkins, 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.
Journal of Medical Genetics|February 11, 1990
Linkage analysis in Marfan syndromeR C Schwartz, S H Blanton, C A Hyde, et al.
Pageof 6