A genetic explanation for the rising incidence of type 1 diabetes, a polygenic disease von Awdeh, Z.L., Yunis, Edmond J., Audeh, Mark J., Fici, Dolores, Pugliese, Alberto, Larsen, Charles E., Alper, Chester A.

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Mendelian inheritance of polygenic diseases: a hypothetical basis for increasing incidence von Awdeh, Z.L., Alper, Chester A.

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Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac disease von 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

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Extended HLA/Complement Allele Haplotypes: Evidence for T/t-Like Complex in Man von Awdeh, Z. L., Raum, D., Yunis, E. J., Alper, C. A.

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Inherited Structural Polymorphism of the Fourth Component of Human Complement von Awdeh, Zuheir L., Alper, Chester A.

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Hepatitis B surface antigen- and tetanus toxoid-specific clonal expansion of CD4+ cells in vitro determined by TCRBV CDR3 length and nucleotide sequence von UKO, G. P, FRASER, P. A, AWDEH, Z. L, FICI, D. A, CRAWFORD, K. D, LARSEN, C. E, ALPER, C. A

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The Paternally Inherited Insulin Gene B Allele (1,428 FokI site) Confers Protection from Insulin-dependent Diabetes in Families von Pugliese, Alberto, Awdeh, Zuheir L., Alper, Chester A., Jackson, Richard A., Eisenbarth, George S.

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Characterization of type I complement C2 deficiency MHC haplotypes. Strong conservation of the complotype/HLA-B-region and absence of disease association due to linked class II gen... von Truedsson, L, Alper, CA, Awdeh, ZL, Johansen, P, Sjoholm, AG, Sturfelt, G

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Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks von Yunis, E.J., Larsen, C.E., Fernandez-Viña, M., Awdeh, Z.L., Romero, T., Hansen, J.A., Alper, C.A.

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Genetic polymorphism of human complement C4 and detection of heterozygotes von Awdeh, Z. L, Raum, D, Alper, C. A

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Isoelectric Focusing in Polyacrylamide Gel and its Application to Immunoglobulins von AWDEH, Z. L, WILLIAMSON, A. R, ASKONAS, BRIGITTE A

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Association of polymorphisms in the HLA-B region with extended haplotypes von EGEA, G. E, YUNIS, I, SPIES, T, STROMINGER, J, AWDEH, Z. L, ALPER, C. A, YUNIS, E. J

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Linkage disequilibrium between HLA-DPB1 alleles and retinoid X receptor β haplotypes von Rajsbaum, Ricardo, Fici, Dolores, Boggs, Deborah A, Fraser, Patricia A, Flores-Villanueva, Pedro O, Awdeh, Zuheir L

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Molecular analysis distinguishes two HLA-DR3-bearing major histocompatibility complex extended haplotypes von WESCOTT, M. Z, AWDEH, Z. L, YUNIS, E. J, ALPER, C. A

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The MHC type 1 diabetes susceptibility gene is centromeric to HLA-DQB1 von Husain, Zaheed, Kelly, M. Ann, Eisenbarth, George S, Pugliese, Alberto, Awdeh, Zuheir L, Larsen, Charles E, Alper, Chester A

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Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency von LAYRISSE, Z, WHITE, C, GUNCZLER, P, GAFARO VALERA, L, ARIAS, S, YUNIS, E. J, ALPER, C. A, AWDEH, Z. L

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MHC determinants of response to Rh immunization von Raum, DD, Awdeh, ZL, Page, PL, Yunis, EJ, Alper, CA

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C4B gene polymorphisms among African and African-American HLA-Bw42-DRw18 haplotypes von FRASER, P. A, AWDEH, Z. L, RONCO, P, SIMON, S, MOORE, B, FICI, D, MARCUS-BAGLEY, D, YUNIS, E. J, ALPER, C. A

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A DNA oligonucleotide microarray for detecting human astrovirus serotypes von Brown, David W., Gunning, Kerry B., Henry, Dorothy M., Awdeh, Zuheir L., Brinker, James P., Tzipori, Saul, Herrmann, John E.

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One cell-one immunoglobulin. Origin of limited heterogeneity of myeloma proteins von Awdeh, Z L, Williamson, A R, Askonas, B A

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