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A F Wright

Showing results (121-130 of 137) with videos related to

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Genomics|January 1, 1990
No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneityC F Inglehearn, M Jay, D H Lester, et al.
American Journal of Human Genetics|September 29, 2000
Pitfalls in homozygosity mappingM G Miano, S G Jacobson, A Carothers, et al.
Human Genetics|January 1, 1993
A study of genetic linkage heterogeneity in 35 adult-onset polycystic kidney disease familiesA F Wright, P W Teague, S E Pound, et al.
Nature|May 17, 1984
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28S S Bhattacharya, A F Wright, J F Clayton, et al.
American Journal of Medical Genetics|June 19, 1995
Automated linkage analysis in psychiatric disordersL He, D C Mansfield, A F Brown, et al.
American Journal of Human Genetics|July 1, 1996
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3R Fujita, E Bingham, P Forsythe, et al.
Gene Therapy|September 9, 2015
Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosaB S Pawlyk, O V Bulgakov, X Sun, et al.
Human Molecular Genetics|March 18, 2005
RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosminX Shu, A M Fry, B Tulloch, et al.
Genomics|April 1, 1997
Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21E A Bruford, R Riise, P W Teague, et al.
Nature Genetics|April 1, 1996
A locus for bipolar affective disorder on chromosome 4pD H Blackwood, L He, S W Morris, et al.
Pageof 14

Showing results (121-130 of 137) with videos related to

Sort By:
Pageof 14
Genomics|January 1, 1990
No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneityC F Inglehearn, M Jay, D H Lester, et al.
American Journal of Human Genetics|September 29, 2000
Pitfalls in homozygosity mappingM G Miano, S G Jacobson, A Carothers, et al.
Human Genetics|January 1, 1993
A study of genetic linkage heterogeneity in 35 adult-onset polycystic kidney disease familiesA F Wright, P W Teague, S E Pound, et al.
Nature|May 17, 1984
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28S S Bhattacharya, A F Wright, J F Clayton, et al.
American Journal of Medical Genetics|June 19, 1995
Automated linkage analysis in psychiatric disordersL He, D C Mansfield, A F Brown, et al.
American Journal of Human Genetics|July 1, 1996
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3R Fujita, E Bingham, P Forsythe, et al.
Gene Therapy|September 9, 2015
Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosaB S Pawlyk, O V Bulgakov, X Sun, et al.
Human Molecular Genetics|March 18, 2005
RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosminX Shu, A M Fry, B Tulloch, et al.
Genomics|April 1, 1997
Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21E A Bruford, R Riise, P W Teague, et al.
Nature Genetics|April 1, 1996
A locus for bipolar affective disorder on chromosome 4pD H Blackwood, L He, S W Morris, et al.
Pageof 14