Bo Dupont

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.

J. Strominger, P. White, D. Chaplin, 1985, Proceedings of the National Academy of Sciences of the United States of America.

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.

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.

P. White, M. New, B. Dupont, 1988, Proceedings of the National Academy of Sciences of the United States of America.

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.