LORENZEN, FRANZISKA

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

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

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

Improved test to identify heterozygotes for congenital adrenal hyperplasia without index case examination

Peter, M., Sippell, W. G., Lorenzen, F., Westphal, E., Willig, R. P., & Grosse-Wilde, H. (1990) · The Lancet

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 41