W Hoepffner

Phenotypic classification of male pseudohermaphroditism due to steroid 5α-reductase 2 deficiency

Gernot H.G. Sinnecker, Olaf Hiort, L. Dibbelt et al. · American Journal of Medical Genetics · 1996 · 184 citations

Copy number variation of two separate regulatory regions upstream of <i>SOX9</i> causes isolated 46,XY or 46,XX disorder of sex development

Gwang-Jin Kim, Elisabeth Sock, Astrid Buchberger et al. · Journal of Medical Genetics · 2015 · 108 citations

Complete virilization in congenital adrenal hyperplasia: clinical course, medical management and disease‐related complications

Joachim Woelfle, W Hoepffner, W.G. Sippell et al. · Clinical Endocrinology · 2002 · 63 citations

Pregnancies in patients with congenital adrenal hyperplasia with complete or almost complete impairment of 21-hydroxylase activity

W Hoepffner, Egbert Schulze, J Bennek et al. · Fertility and Sterility · 2004 · 62 citations · Full text

Adrenal Gland, Urology, 21-Hydroxylase Activity +10

Divergence between genotype and phenotype in relatives of patients with the intron 2 mutation of steroid-21-hydroxylase

E Schulze, Gunter Scharer, A. Rogatzki et al. · Endocrine Research · 1995 · 48 citations