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S P Daiger

Showing results (51-60 of 84) with videos related to

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Human Genetics|May 1, 1987
Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuriaR Chakraborty, A S Lidsky, S P Daiger, 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.
American Journal of Human Genetics|July 1, 1997
Exclusion of atypical vitelliform macular dystrophy from 8q24.3 and from other known macular degenerative lociM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.
Annals of Neurology|June 1, 1988
Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindredH Y Zoghbi, M S Pollack, L A Lyons, et al.
American Journal of Human Genetics|February 1, 1989
Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysisH Y Zoghbi, L A Sandkuyl, J Ott, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX geneR T Tzekov, Y Liu, M M Sohocki, et al.
Genome Research|April 1, 1996
Mapping the RP10 locus for autosomal dominant retinitis pigmentosa on 7q: refined genetic positioning and localization within a well-defined YAC contigR E McGuire, S A Jordan, V V Braden, et al.
American Journal of Human Genetics|July 1, 1985
Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuriaA S Lidsky, F D Ledley, A G DiLella, 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.
Nucleic Acids Research|March 25, 1992
A tight linkage cluster, with two new RFLPs (D8S96 and D8S108), in the interval 8cen-q13A W Cottingham, L A Sadler, S H Blanton, et al.
Pageof 9

Showing results (51-60 of 84) with videos related to

Sort By:
Pageof 9
Human Genetics|May 1, 1987
Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuriaR Chakraborty, A S Lidsky, S P Daiger, 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.
American Journal of Human Genetics|July 1, 1997
Exclusion of atypical vitelliform macular dystrophy from 8q24.3 and from other known macular degenerative lociM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.
Annals of Neurology|June 1, 1988
Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindredH Y Zoghbi, M S Pollack, L A Lyons, et al.
American Journal of Human Genetics|February 1, 1989
Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysisH Y Zoghbi, L A Sandkuyl, J Ott, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX geneR T Tzekov, Y Liu, M M Sohocki, et al.
Genome Research|April 1, 1996
Mapping the RP10 locus for autosomal dominant retinitis pigmentosa on 7q: refined genetic positioning and localization within a well-defined YAC contigR E McGuire, S A Jordan, V V Braden, et al.
American Journal of Human Genetics|July 1, 1985
Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuriaA S Lidsky, F D Ledley, A G DiLella, 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.
Nucleic Acids Research|March 25, 1992
A tight linkage cluster, with two new RFLPs (D8S96 and D8S108), in the interval 8cen-q13A W Cottingham, L A Sadler, S H Blanton, et al.
Pageof 9