Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac disease
Bilbao, J R, Calvo, B, Aransay, A M, Martin-Pagola, A, Perez de Nanclares, G, Aly, T A, Rica, I, Vitoria, J C, Gaztambide, S, Noble, J, Fain, P R, Awdeh, Z L, Alper, C A, Castaño, L
Published in Genes and immunity (01.10.2006)
Published in Genes and immunity (01.10.2006)
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X-Linked Syndrome of Polyendocrinopathy, Immune Dysfunction, and Diarrhea Maps to Xp11.23-Xq13.3
Bennett, Craig L., Yoshioka, Ritsuko, Kiyosawa, Hidenori, Barker, David F., Fain, Pamela R., Shigeoka, Ann O., Chance, Phillip F.
Published in American journal of human genetics (01.02.2000)
Published in American journal of human genetics (01.02.2000)
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Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia
Cambi, F, Tang, X M, Cordray, P, Fain, P R, Keppen, L D, Barker, D F
Published in Neurology (01.04.1996)
Published in Neurology (01.04.1996)
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Transmission of DQ haplotypes to patients with type 1 diabetes
KAWASAKI, E, NOBLE, J, ERLICH, H, MULGREW, C. L, FAIN, P. R, EISENBARTH, G. S
Published in Diabetes (New York, N.Y.) (01.12.1998)
Published in Diabetes (New York, N.Y.) (01.12.1998)
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A 2D crossover-based map of the human X chromosome as a model for map integration
Chance, Phillip F, Nguyen, Kim, Econs, Michael J, Kort, Edward N, Redd, Douglas F, Fain, Pamela R, Barker, David F
Published in Nature genetics (01.03.1995)
Published in Nature genetics (01.03.1995)
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A High Resolution CEPH Crossover Mapping Panel and Integrated Map of Chromosome 11
Fain, Pamela R., Kort, Edward N., Yousry, Cherine, James, Michael R., Litt, Michael
Published in Human molecular genetics (01.10.1996)
Published in Human molecular genetics (01.10.1996)
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A genetic map of human chromosome 17p
Wright, E.C., Goldgar, D.E., Fain, P.R., Barker, D.F., Skolnick, M.H.
Published in Genomics (San Diego, Calif.) (01.05.1990)
Published in Genomics (San Diego, Calif.) (01.05.1990)
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Differential effects of DRB10301 and DQA10501-DQB10201 on the activation and progression of islet cell autoimmunity
Eller, E, Vardi, P, McFann, K K, Babu, S R, Yu, L, Bugawan, T L, Erlich, H A, Eisenbarth, G S, Fain, P R
Published in Genes and immunity (01.12.2007)
Published in Genes and immunity (01.12.2007)
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Linkage Heterogeneity of Autosomal Dominant Polycystic Kidney Disease
Kimberling, William J, Fain, Pamela R, Kenyon, J.B, Goldgar, David, Sujansky, Eva, Gabow, Patricia A
Published in The New England journal of medicine (06.10.1988)
Published in The New England journal of medicine (06.10.1988)
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Fine structure mapping of the human X-linked hypophosphatemic rickets gene locus
Econs, M J, Rowe, P S, Francis, F, Barker, D F, Speer, M C, Norman, M, Fain, P R, Weissenbach, J, Read, A, Davis, K E
Published in The journal of clinical endocrinology and metabolism (01.11.1994)
Published in The journal of clinical endocrinology and metabolism (01.11.1994)
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BRCA1 R841W: A strong candidate for a common mutation with moderate phenotype
Barker, David F., Almeida, Eduardo R.A., Casey, Graham, Fain, Pamela R., Liao, Shu-Yuan, Masunaka, Irene, Noble, Barbara, Kurosaki, Tom, Anton-Culver, Hoda
Published in Genetic epidemiology (1996)
Published in Genetic epidemiology (1996)
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A Genomewide Screen for Generalized Vitiligo: Confirmation of AIS1 on Chromosome 1p31 and Evidence for Additional Susceptibility Loci
Fain, Pamela R., Gowan, Katherine, LaBerge, Greggory S., Alkhateeb, Asem, Stetler, Gary L., Talbert, Janet, Bennett, Dorothy C., Spritz, Richard A.
Published in American journal of human genetics (01.06.2003)
Published in American journal of human genetics (01.06.2003)
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