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A F Wright

Showing results (111-120 of 137) with videos related to

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Journal of Medical Genetics|July 1, 1991
Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindredA F Wright, S S Bhattacharya, M A Aldred, et al.
Journal of Medical Genetics|March 1, 1995
Haplotype analysis in autosomal dominant polycystic kidney diseaseS E Pound, S Thomas, A Snarey, et al.
American Journal of Human Genetics|September 1, 1990
Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneityD H Lester, C F Inglehearn, R Bashir, et al.
American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)A Snarey, S Thomas, M C Schneider, et al.
Cell Biophysics|January 1, 1993
Antitumor effects of an antibody-carboxypeptidase G2 conjugate in combination with a benzoic acid mustard prodrugD C Blakey, B E Valcaccia, S East, et al.
Heredity|December 24, 2015
Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populationsM Shirali, R Pong-Wong, P Navarro, et al.
American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, et al.
Scientific Reports|May 20, 2015
Application of high-dimensional feature selection: evaluation for genomic prediction in manM L Bermingham, R Pong-Wong, A Spiliopoulou, et al.
Human Molecular Genetics|November 14, 2003
Extent of linkage disequilibrium in a Sardinian sub-isolate: sampling and methodological considerationsA Tenesa, A F Wright, S A Knott, et al.
Psychiatric Genetics|January 1, 1996
Recombination patterns around the breakpoints of a balanced 1;11 autosomal translocation associated with major mental illnessL He, A Carothers, D H Blackwood, et al.
Pageof 14

Showing results (111-120 of 137) with videos related to

Sort By:
Pageof 14
Journal of Medical Genetics|July 1, 1991
Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindredA F Wright, S S Bhattacharya, M A Aldred, et al.
Journal of Medical Genetics|March 1, 1995
Haplotype analysis in autosomal dominant polycystic kidney diseaseS E Pound, S Thomas, A Snarey, et al.
American Journal of Human Genetics|September 1, 1990
Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneityD H Lester, C F Inglehearn, R Bashir, et al.
American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1)A Snarey, S Thomas, M C Schneider, et al.
Cell Biophysics|January 1, 1993
Antitumor effects of an antibody-carboxypeptidase G2 conjugate in combination with a benzoic acid mustard prodrugD C Blakey, B E Valcaccia, S East, et al.
Heredity|December 24, 2015
Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populationsM Shirali, R Pong-Wong, P Navarro, et al.
American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, et al.
Scientific Reports|May 20, 2015
Application of high-dimensional feature selection: evaluation for genomic prediction in manM L Bermingham, R Pong-Wong, A Spiliopoulou, et al.
Human Molecular Genetics|November 14, 2003
Extent of linkage disequilibrium in a Sardinian sub-isolate: sampling and methodological considerationsA Tenesa, A F Wright, S A Knott, et al.
Psychiatric Genetics|January 1, 1996
Recombination patterns around the breakpoints of a balanced 1;11 autosomal translocation associated with major mental illnessL He, A Carothers, D H Blackwood, et al.
Pageof 14