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S S Papiha

Showing results (131-140 of 144) with videos related to

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Progress in Clinical and Biological Research|January 1, 1989
X-linked retinitis pigmentosa: a molecular genetic approach to isolating the defective genesS Lindsay, M Jay, D J Bower, et al.
Human Genetics|January 1, 1983
The associations of HLA and other genetic markers with glomerulonephritisH U Rashid, S S Papiha, B Agroyannis, et al.
Tubercle|September 1, 1987
Association of HLA and other genetic markers in South Indian patients with pulmonary tuberculosisS S Papiha, B N Singh, J S Lanchbury, et al.
Kidney International|January 1, 1987
HLA-A, B, DR and Bf allotypes in patients with idiopathic membranous nephropathy (IMN)S S Papiha, S K Pareek, R S Rodger, et al.
Diabetes Care|August 1, 1996
Lack of diabetes in rural Colombian AmerindiansI Briceño, L A Barriocanal, S S Papiha, et al.
Human Genetics|January 1, 1983
The polymorphism of the vitamin D-binding protein (Gc); isoelectric focusing in 3 M urea as additional method for identification of genetic variantsJ Constans, H Cleve, D Dykes, et al.
Psychiatric Genetics|January 1, 1996
Reduced expression of HLA-B35 in schizophreniaD H Blackwood, W J Muir, A Stephenson, 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.
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.
Human Biology|May 10, 2000
Distribution of the 3' VNTR polymorphism in the human dopamine transporter gene in world populationsR J Mitchell, S Howlett, L Earl, et al.
Pageof 15

Showing results (131-140 of 144) with videos related to

Sort By:
Pageof 15
Progress in Clinical and Biological Research|January 1, 1989
X-linked retinitis pigmentosa: a molecular genetic approach to isolating the defective genesS Lindsay, M Jay, D J Bower, et al.
Human Genetics|January 1, 1983
The associations of HLA and other genetic markers with glomerulonephritisH U Rashid, S S Papiha, B Agroyannis, et al.
Tubercle|September 1, 1987
Association of HLA and other genetic markers in South Indian patients with pulmonary tuberculosisS S Papiha, B N Singh, J S Lanchbury, et al.
Kidney International|January 1, 1987
HLA-A, B, DR and Bf allotypes in patients with idiopathic membranous nephropathy (IMN)S S Papiha, S K Pareek, R S Rodger, et al.
Diabetes Care|August 1, 1996
Lack of diabetes in rural Colombian AmerindiansI Briceño, L A Barriocanal, S S Papiha, et al.
Human Genetics|January 1, 1983
The polymorphism of the vitamin D-binding protein (Gc); isoelectric focusing in 3 M urea as additional method for identification of genetic variantsJ Constans, H Cleve, D Dykes, et al.
Psychiatric Genetics|January 1, 1996
Reduced expression of HLA-B35 in schizophreniaD H Blackwood, W J Muir, A Stephenson, 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.
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.
Human Biology|May 10, 2000
Distribution of the 3' VNTR polymorphism in the human dopamine transporter gene in world populationsR J Mitchell, S Howlett, L Earl, et al.
Pageof 15