Dupont, B

Genotyping steroid 21-hydroxylase deficiency: hormonal reference data

NEW, M. I., LORENZEN, F., LERNER, A. J., KOHN, B., OBERFIELD, S. E., POLLACK, M. S., DUPONT, B., STONER, E., LEVY, D. J., PANG, S., et al. (1983) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 624

Structure of human steroid 21-hydroxylase genes.

White, P. C., New, M. I., & Dupont, B. (1986) · Proceedings of the National Academy of Sciences

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 569

High frequency of nonclassical steroid 21-hydroxylase deficiency

SPEISER, P. W., DUPONT, B. O., RUBINSTEIN, P., PIAZZA, A., KASTELAN, A., & NEW, M. I. (1986) · Obstetrical & Gynecological Survey

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 523

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

White, P. C., Grossberger, D., Onufer, B. J., Chaplin, D. D., New, M. I., Dupont, B., & Strominger, J. L. (1985) · Proceedings of the National Academy of Sciences

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 490

Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency)

Dupont, B., Oberfield, S. E., Smithwick, E. M., Lee, T. D., & Levine, L. S. (1977) · The Lancet

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 371

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.

White, P. C., New, M. I., & Dupont, B. (1984) · Proceedings of the National Academy of Sciences

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 292

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

White, P. C., Vitek, A., Dupont, B., & New, M. I. (1988) · Proceedings of the National Academy of Sciences

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 229

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

KOHN, B., LEVINE, L. S., POLLACK, M. S., PANG, S., LORENZEN, F., LEVY, D., LERNER, A. J., RONDANINI, G. F., DUPONT, B., & NEW, M. I. (1982) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 204

Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing

Pollack, M. S., Levine, L. S., Pang, S., Owens, R. P., Nitowsky, H. M., Dupont, B., Maurer, D., New, M. I., Duchon, M., Merkatz, I. R., et al. (1979) · The Lancet

Sexual Differentiation and DisordersPrenatal Screening and Diagnostics

Cited by 126

Nonsalt-losing congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency with normal glomerulosa function

Pang, S., Levine, L. S., Stoner, E., Opitz, J. M., Pollack, M. S., Dupont, B., & New, M. I. (1983) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 112

Genetic and Hormonal Characterization of Cryptic 21-Hydroxylase Deficiency*

LEVINE, L. S., DUPONT, B., LORENZEN, F., PANG, S., POLLACK, M., OBERFIELD, S. E., KOHN, B., LERNER, A., CACCIARI, E., MANTERO, F., et al. (1981) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 81