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S P Daiger

Showing results (31-40 of 84) with videos related to

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The American Journal of Cardiology|November 1, 1982
Familial aggregation of coronary heart disease and its relation to known genetic risk factorsL P ten Kate, H Boman, S P Daiger, et al.
American Journal of Human Genetics|July 1, 1984
Multiple, independent restriction site polymorphisms in human DNA detected with a cDNA probe to argininosuccinate synthetase (AS)S P Daiger, N S Hoffman, R S Wildin, et al.
Biochemical Genetics|February 1, 1984
X-linked, polymorphic genetic variation of thyroxin-binding globulin (TBG) in baboons and screening of additional primatesD H Lockwood, D H Coppenhaver, R E Ferrell, et al.
Genomics|May 20, 1999
Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disordersM M Sohocki, K A Malone, L S Sullivan, et al.
Human Genetics|December 1, 1996
Genetic mapping of RP1 on 8q11-q21 in an Australian family with autosomal dominant retinitis pigmentosa reduces the critical region to 4 cM between D8S601 and D8S285S Y Xu, M Denton, L Sullivan, et al.
Human Mutation|January 1, 1993
A leucine to arginine amino acid substitution at codon 46 of rhodopsin is responsible for a severe form of autosomal dominant retinitis pigmentosaJ A Rodriguez, C A Herrera, D G Birch, et al.
The New England Journal of Medicine|March 23, 1978
Vitamin-D-binding protein in the Williams syndrome and idiopathic hypercalcemiaS P Daiger, M Miller, G Romeo, 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|June 1, 1988
Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLAH Y Zoghbi, S P Daiger, A McCall, et al.
Nucleic Acids Research|September 11, 1991
A new StyI RFLP and haplotypes with the HindIII RFLP at the D8S5 (TL11) locusA W Cottingham, S H Blanton, A E Retief, et al.
Pageof 9

Showing results (31-40 of 84) with videos related to

Sort By:
Pageof 9
The American Journal of Cardiology|November 1, 1982
Familial aggregation of coronary heart disease and its relation to known genetic risk factorsL P ten Kate, H Boman, S P Daiger, et al.
American Journal of Human Genetics|July 1, 1984
Multiple, independent restriction site polymorphisms in human DNA detected with a cDNA probe to argininosuccinate synthetase (AS)S P Daiger, N S Hoffman, R S Wildin, et al.
Biochemical Genetics|February 1, 1984
X-linked, polymorphic genetic variation of thyroxin-binding globulin (TBG) in baboons and screening of additional primatesD H Lockwood, D H Coppenhaver, R E Ferrell, et al.
Genomics|May 20, 1999
Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disordersM M Sohocki, K A Malone, L S Sullivan, et al.
Human Genetics|December 1, 1996
Genetic mapping of RP1 on 8q11-q21 in an Australian family with autosomal dominant retinitis pigmentosa reduces the critical region to 4 cM between D8S601 and D8S285S Y Xu, M Denton, L Sullivan, et al.
Human Mutation|January 1, 1993
A leucine to arginine amino acid substitution at codon 46 of rhodopsin is responsible for a severe form of autosomal dominant retinitis pigmentosaJ A Rodriguez, C A Herrera, D G Birch, et al.
The New England Journal of Medicine|March 23, 1978
Vitamin-D-binding protein in the Williams syndrome and idiopathic hypercalcemiaS P Daiger, M Miller, G Romeo, 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|June 1, 1988
Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLAH Y Zoghbi, S P Daiger, A McCall, et al.
Nucleic Acids Research|September 11, 1991
A new StyI RFLP and haplotypes with the HindIII RFLP at the D8S5 (TL11) locusA W Cottingham, S H Blanton, A E Retief, et al.
Pageof 9