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1

Association between phosphoglucomutase (PGM1) and group-specific component (Gc) subtypes and tuberculosis. 著者: Papiha, S S, Agarwal, S S, White, I

出版事項 1983

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2

Genetic structure of the population with rheumatoid arthritis in north east England: a genetic approach to define different subtypes. 著者: Papiha, S S, Lanchbury, J S, Pal, B

出版事項 1986

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3

Response of human peripheral blood lymphocytes in the presence of cord sera: relationship of lymphocyte transformation with number of pregnancies and levels of alpha-fetoprotein. 著者: Wajner, M, Papiha, S S, Wagstaff, T I

出版事項 1983

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4

Relationship between serum immunoglobulin G and alpha-fetoprotein levels during human pregnancy 著者: Moacır Wajner, S.S. Papiha, T. I. Wagstaff

出版事項 1987

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Artigo

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5

Relationship between some obstetric landmarks and the concentration of alpha-fetoprotein in maternal blood 著者: Moacır Wajner, S.S. Papiha, Thomes Jan Wagstaff

出版事項 1986

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Artigo

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6

Polymorphisms and multiple sclerosis in Orkney. 著者: Roberts, D F, Papiha, S S, Poskanzer, D C

出版事項 1979

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7

Immunoglobulin levels in Iraq. 著者: Al-Agidi, S K, Papiha, S S, Roberts, D F

出版事項 1977

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8

Red cell enzyme polymorphisms in Ceylon Sinhalese. 著者: Roberts, D F, Papiha, S S, Abeyaratne, K P

出版事項 1972

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9

A rare homozygous form of phosphohexose isomerase. 著者: Papiha, S S, Roberts, D F, Chhaparwal, B C

出版事項 1974

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10

Haptoglobins in chronic lymphatic leukaemia 著者: Papiha, S. S., Jones, A. L., Thompson, B., Carr, D.

出版事項 1974

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11

Genetic differentiation among Iranian Christian communities. 著者: Akbari, M T, Papiha, S S, Roberts, D F, Farhud, D D

出版事項 1986

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12

Alpha 1 antitrypsin (PI) phenotypes in two rheumatic diseases: a reappraisal of the association of PI subtypes in rheumatoid arthritis. 著者: Papiha, S S, Pal, B, Walker, D, Mangion, P, Hossain, M A

出版事項 1989

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13

Age related somatic mitochondrial DNA deletions in bone. 著者: Papiha, S S, Rathod, H, Briceno, I, Pooley, J, Datta, H K

出版事項 1998

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14

Association of HLA-DRB1 alleles with giant cell tumour of bone. 著者: Varanasi, S S, Athanasou, N A, Briceno, I, Papiha, S S, Datta, H K

出版事項 1999

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15

Association of Wegener's granulomatosis with HLA antigens and other genetic markers. 著者: Papiha, S S, Murty, G E, Ad'Hia, A, Mains, B T, Venning, M

出版事項 1992

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16

Population frequencies of three DNA alleles linked to the Duchenne muscular dystrophy gene. 著者: Papiha, S S, Roberts, D F, Clarke, A, Burn, J, Gardner-Medwin, D, Bhattacharya, S S

出版事項 1989

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17

Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus. 著者: Inglehearn, C F, Papiha, S S, Jay, M, Wright, A F, Moore, A T, Bhattacharya, S S

出版事項 1990

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18

The Emerging Limbs and Twigs of the East Asian mtDNA Tree 著者: Toomas Kivisild, Helle-Viivi Tolk, Jüri Parik, Yiming Wang, S.S. Papiha, Hans‐Jürgen Bandelt, Richard Villems

出版事項 2002

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Artigo

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19

Functional contribution of the intestinal microbiome in autism spectrum disorder, attention deficit hyperactivity disorder, and Rett syndrome: a systematic review of pediatric and... 著者: Valentina Caputi, Lee Hill, Melanie Figueiredo, Jelena Popov, Emily Hartung, Kara Gross Margolis, Kanish Baskaran, Papiha Joharapurkar, Michal Moshkovich, Nikhil Pai

出版事項 2024

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Revisão

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20

Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity. 著者: Lester, D H, Inglehearn, C F, Bashir, R, Ackford, H, Esakowitz, L, Jay, M, Bird, A C, Wright, A F, Papiha, S S, Bhattacharya, S S

出版事項 1990

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検索結果 - S.S. Papiha

Association between phosphoglucomutase (PGM1) and group-specific component (Gc) subtypes and tuberculosis. 著者: Papiha, S S, Agarwal, S S, White, I

Genetic structure of the population with rheumatoid arthritis in north east England: a genetic approach to define different subtypes. 著者: Papiha, S S, Lanchbury, J S, Pal, B

Response of human peripheral blood lymphocytes in the presence of cord sera: relationship of lymphocyte transformation with number of pregnancies and levels of alpha-fetoprotein. 著者: Wajner, M, Papiha, S S, Wagstaff, T I

Relationship between serum immunoglobulin G and alpha-fetoprotein levels during human pregnancy 著者: Moacır Wajner, S.S. Papiha, T. I. Wagstaff

Relationship between some obstetric landmarks and the concentration of alpha-fetoprotein in maternal blood 著者: Moacır Wajner, S.S. Papiha, Thomes Jan Wagstaff

Polymorphisms and multiple sclerosis in Orkney. 著者: Roberts, D F, Papiha, S S, Poskanzer, D C

Immunoglobulin levels in Iraq. 著者: Al-Agidi, S K, Papiha, S S, Roberts, D F

Red cell enzyme polymorphisms in Ceylon Sinhalese. 著者: Roberts, D F, Papiha, S S, Abeyaratne, K P

A rare homozygous form of phosphohexose isomerase. 著者: Papiha, S S, Roberts, D F, Chhaparwal, B C

Haptoglobins in chronic lymphatic leukaemia 著者: Papiha, S. S., Jones, A. L., Thompson, B., Carr, D.

Genetic differentiation among Iranian Christian communities. 著者: Akbari, M T, Papiha, S S, Roberts, D F, Farhud, D D

Alpha 1 antitrypsin (PI) phenotypes in two rheumatic diseases: a reappraisal of the association of PI subtypes in rheumatoid arthritis. 著者: Papiha, S S, Pal, B, Walker, D, Mangion, P, Hossain, M A

Age related somatic mitochondrial DNA deletions in bone. 著者: Papiha, S S, Rathod, H, Briceno, I, Pooley, J, Datta, H K

Association of HLA-DRB1 alleles with giant cell tumour of bone. 著者: Varanasi, S S, Athanasou, N A, Briceno, I, Papiha, S S, Datta, H K

Association of Wegener's granulomatosis with HLA antigens and other genetic markers. 著者: Papiha, S S, Murty, G E, Ad'Hia, A, Mains, B T, Venning, M

Population frequencies of three DNA alleles linked to the Duchenne muscular dystrophy gene. 著者: Papiha, S S, Roberts, D F, Clarke, A, Burn, J, Gardner-Medwin, D, Bhattacharya, S S

Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus. 著者: Inglehearn, C F, Papiha, S S, Jay, M, Wright, A F, Moore, A T, Bhattacharya, S S

The Emerging Limbs and Twigs of the East Asian mtDNA Tree 著者: Toomas Kivisild, Helle-Viivi Tolk, Jüri Parik, Yiming Wang, S.S. Papiha, Hans‐Jürgen Bandelt, Richard Villems

Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity. 著者: Lester, D H, Inglehearn, C F, Bashir, R, Ackford, H, Esakowitz, L, Jay, M, Bird, A C, Wright, A F, Papiha, S S, Bhattacharya, S S

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