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S P Daiger

Showing results (61-70 of 84) with videos related to

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American Journal of Human Genetics|August 1, 1989
Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU)S P Daiger, R Chakraborty, L Reed, et al.
Genomics|March 1, 1997
Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sitesM M Sohocki, L S Sullivan, W R Harrison, 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.
Molecular Vision|March 9, 2000
Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7qS J Bowne, L S Sullivan, L Ding, et al.
Eye (London, England)|November 7, 2009
Long-term follow-up of a family with dominant X-linked retinitis pigmentosaD M Wu, H Khanna, P Atmaca-Sonmez, et al.
American Journal of Human Genetics|May 1, 1989
Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and SwitzerlandS E Sullivan, S D Moore, J M Connor, 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 Human Genetics|August 1, 1989
Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU)S P Daiger, L Reed, S S Huang, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groupsS P Daiger, M M Humphries, N Giesenschlag, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Exclusion of Usher syndrome gene from much of chromosome 4R J Smith, J D Holcomb, S P Daiger, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|August 1, 1989
Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU)S P Daiger, R Chakraborty, L Reed, et al.
Genomics|March 1, 1997
Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sitesM M Sohocki, L S Sullivan, W R Harrison, 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.
Molecular Vision|March 9, 2000
Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7qS J Bowne, L S Sullivan, L Ding, et al.
Eye (London, England)|November 7, 2009
Long-term follow-up of a family with dominant X-linked retinitis pigmentosaD M Wu, H Khanna, P Atmaca-Sonmez, et al.
American Journal of Human Genetics|May 1, 1989
Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and SwitzerlandS E Sullivan, S D Moore, J M Connor, 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 Human Genetics|August 1, 1989
Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU)S P Daiger, L Reed, S S Huang, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groupsS P Daiger, M M Humphries, N Giesenschlag, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Exclusion of Usher syndrome gene from much of chromosome 4R J Smith, J D Holcomb, S P Daiger, et al.
Pageof 9