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S H Blanton

Showing results (31-40 of 53) with videos related to

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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 24, 1997
Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24R W Yee, L S Sullivan, H T Lai, 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.
American Journal of Human Genetics|October 11, 1992
Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhereH Northrup, D J Kwiatkowski, E S Roach, 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.
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 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
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 24, 1997
Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24R W Yee, L S Sullivan, H T Lai, 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.
American Journal of Human Genetics|October 11, 1992
Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhereH Northrup, D J Kwiatkowski, E S Roach, 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.
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 6