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S H Blanton

Showing results (21-30 of 53) with videos related to

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American Journal of Veterinary Research|January 1, 1997
Linkage of a microsatellite marker to the canine copper toxicosis locus in Bedlington terriersV Yuzbasiyan-Gurkan, S H Blanton, Y Cao, et al.
American Journal of Human Genetics|June 1, 1996
Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversionV Shashi, W L Golden, P S Allinson, et al.
Genomics|June 14, 2000
Confirmation of the mapping of the Camurati-Englemann locus to 19q13. 2 and refinement to a 3.2-cM regionS P Vaughn, S Broussard, C R Hall, et al.
American Journal of Medical Genetics|July 13, 2002
Testing for genetic associations with the PAX gene family in a spina bifida populationK A Volcik, S H Blanton, M C Kruzel, et al.
American Journal of Medical Genetics|July 13, 2002
Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defectsK A Volcik, S H Blanton, M C Kruzel, et al.
Human Genetics|June 21, 2001
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in CaucasiansM Tekin, N Akar, S Cin, 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.
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.
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.
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.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
American Journal of Veterinary Research|January 1, 1997
Linkage of a microsatellite marker to the canine copper toxicosis locus in Bedlington terriersV Yuzbasiyan-Gurkan, S H Blanton, Y Cao, et al.
American Journal of Human Genetics|June 1, 1996
Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversionV Shashi, W L Golden, P S Allinson, et al.
Genomics|June 14, 2000
Confirmation of the mapping of the Camurati-Englemann locus to 19q13. 2 and refinement to a 3.2-cM regionS P Vaughn, S Broussard, C R Hall, et al.
American Journal of Medical Genetics|July 13, 2002
Testing for genetic associations with the PAX gene family in a spina bifida populationK A Volcik, S H Blanton, M C Kruzel, et al.
American Journal of Medical Genetics|July 13, 2002
Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defectsK A Volcik, S H Blanton, M C Kruzel, et al.
Human Genetics|June 21, 2001
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in CaucasiansM Tekin, N Akar, S Cin, 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.
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.
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.
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.
Pageof 6