Inherited structural polymorphism of the fourth component of human complement.

Yazar: Awdeh, Z L, Alper, C A
Baskı/Yayın Bilgisi 1980

Regulation of monoclonal immunoglobulin G synthesis by antiidiotypic antibody in a patient with hypogammaglobulinemia.

Yazar: Mudawwar, F, Awdeh, Z, Ault, K, Geha, R S
Baskı/Yayın Bilgisi 1980

Genetic analysis of C4 deficiency.

Yazar: Awdeh, Z L, Ochs, H D, Alper, C A
Baskı/Yayın Bilgisi 1981

One cell–one immunoglobin. Origin of limited heterogeneity of myeloma proteins

Yazar: Awdeh, Z. L., Williamson, A. R., Askonas, Brigitte A.
Baskı/Yayın Bilgisi 1970

The homogenous γG-immunoglobulin produced by mouse plasmacytoma 5563 and its subsequent heterogeneity in serum

Yazar: Awdeh, Z. L., Askonas, Brigitte A., Williamson, Alan R.
Baskı/Yayın Bilgisi 1967

Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man.

Yazar: Awdeh, Z L, Raum, D, Yunis, E J, Alper, C A
Baskı/Yayın Bilgisi 1983

Extended major histocompatibility complex haplotypes in type I diabetes mellitus.

Yazar: Raum, D, Awdeh, Z, Yunis, E J, Alper, C A, Gabbay, K H
Baskı/Yayın Bilgisi 1984

Extended major histocompatibility complex haplotypes in patients with gluten-sensitive enteropathy.

Yazar: Alper, C A, Fleischnick, E, Awdeh, Z, Katz, A J, Yunis, E J
Baskı/Yayın Bilgisi 1987

An unusual "morphologic" variant of BF S.

Yazar: Raum, D, Surgenor, T, Awdeh, Z, Marcus, D, Blumenthal, M, Yunis, E J, Alper, C A
Baskı/Yayın Bilgisi 1984

Association of DQw7 (DQB1*0301) with ocular cicatricial pemphigoid.

Yazar: Ahmed, A R, Foster, S, Zaltas, M, Notani, G, Awdeh, Z, Alper, C A, Yunis, E J
Baskı/Yayın Bilgisi 1991

Major histocompatibility complex haplotypes and class II genes in non-Jewish patients with pemphigus vulgaris.

Yazar: Ahmed, A R, Wagner, R, Khatri, K, Notani, G, Awdeh, Z, Alper, C A, Yunis, E J
Baskı/Yayın Bilgisi 1991

Major histocompatibility complex haplotype studies in Ashkenazi Jewish patients with pemphigus vulgaris.

Yazar: Ahmed, A R, Yunis, E J, Khatri, K, Wagner, R, Notani, G, Awdeh, Z, Alper, C A
Baskı/Yayın Bilgisi 1990

A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes).

Yazar: Simon, S, Awdeh, Z, Campbell, R D, Ronco, P, Brink, S J, Eisenbarth, G S, Yunis, E J, Alper, C A
Baskı/Yayın Bilgisi 1991

Two subsets of HLA-DQA1 alleles mark phenotypic variation in levels of insulin autoantibodies in first degree relatives at risk for insulin-dependent diabetes.

Yazar: Pugliese, A, Bugawan, T, Moromisato, R, Awdeh, Z L, Alper, C A, Jackson, R A, Erlich, H A, Eisenbarth, G S
Baskı/Yayın Bilgisi 1994

Human C4 haplotypes with duplicated C4A or C4B.

Yazar: Raum, D, Awdeh, Z, Anderson, J, Strong, L, Granados, J, Teran, L, Giblett, E, Yunis, E J, Alper, C A
Baskı/Yayın Bilgisi 1984

HLA-DRB1 leprogenic motifs in Nigerian population groups

Yazar: Uko, G P, Lu, L-Y, Asuquo, M A, Fici, D, Mahan, S, Awdeh, Z, Udim, E R, Ding, W, Umana, U, Adewole, T, Fraser, P A
Baskı/Yayın Bilgisi 1999

Complement-human histocompatibility antigen haplotypes in C2 deficiency.

Yazar: Awdeh, Z L, Raum, D D, Glass, D, Agnello, V, Schur, P H, Johnston, R B, Gelfand, E W, Ballow, M, Yunis, E, Alper, C A
Baskı/Yayın Bilgisi 1981