M S Pollack

Uniparental disomy as a mechanism for human genetic disease.

J. Edward Spence, R G Perciaccante, Gillian Greig et al. · PubMed · 1988 · 490 citations

Life Sciences, Genetics, Molecular Genetics +11

PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) BY HLA TYPING

M S Pollack, L S Levine, Songya Pang et al. · The Lancet · 1979 · 128 citations

Medicine, Endocrinology, Obstetrics +14

Frequencies of HLA and Gm immunogenetic markers in Kaposi's sarcoma

M S Pollack, Bijan Safai, Patricia L. Myskowski et al. · Tissue Antigens · 1983 · 99 citations

Life Sciences, Genetics, Immunology +17

HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.

M S Pollack, L S Levine, G. J. O’Neill et al. · PubMed · 1981 · 98 citations

Life Sciences, Genetics, Molecular Genetics +10

Genetic Regulation of the Capacity to Make Immunoglobulin G to Pneumococcal Capsular Polysaccharides

Daniel M. Musher, J. E. Groover, David Watson et al. · Journal of Investigative Medicine · 1997 · 81 citations

Life Sciences, Genetics, Immunology +16