Marilyn S. Pollack

Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.

B. Kohn, M. New, B. Dupont, 1982, The Journal of clinical endocrinology and metabolism.

Genetic and technical aspects of the HLA system and its possible role in human malignancy.

M. Pollack, Marilyn S. Pollack, 1984, Cancer investigation.

Human leukocyte antigen associations in basal cell carcinoma.

B. Safai, B. Dupont, P. Myskowski, 1985, Journal of the American Academy of Dermatology.

DR‐POSITIVE MATERNAL ENGRAFTED T CELLS IN A SEVERE COMBINED IMMUNODEFICIENCY PATIENT WITHOUT GRAFT‐VERSUS-HOST DISEASE

F. Christiansen, S. Kim, B. Dupont, 1980, Transplantation.

Preparing monolayers of non-adherent mammalian cells.

M. Pollack, M. J. Mattes, D. Maurer, 1983, Journal of immunological methods.

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

B. Kohn, M. New, B. Dupont, 1981, American journal of human genetics.

Association of HLA-DR5 with mycosis fungoides.

B. Safai, B. Dupont, P. Myskowski, 1983, The Journal of investigative dermatology.

Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.

B. Kohn, C. Scaroni, M. New, 1980, The Journal of clinical endocrinology and metabolism.