J Glatzl

CYP11B1 mutations causing congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.

Stephan Geley, Klaus Kapelari, Karin Jöhrer et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 127 citations · Full text

Genetics, Pathology, Molecular Genetics +19

Characterization of two point mutations in the androgen receptor gene of patients with perineoscrotal hypospadia

Felizia Kaspar, Andrew C.B. Cato, Anne Denninger et al. · The Journal of Steroid Biochemistry and Molecular Biology · 1993 · 30 citations

Urology, Point Mutations, Female Infertility +9

ANDROGEN RECEPTOR POINT MUTATIONS AS THE UNDERLYING MOLECULAR DEFECT IN 2 PATIENTS WITH ANDROGEN INSENSITIVITY SYNDROME

Christian Radmayr, Zoran Čulig, J Glatzl et al. · The Journal of Urology · 1997 · 30 citations

Hereditary angio-oedema: treatment with danazol.

G Tappeiner, Helmut Hintner, J Glatzl et al. · British Journal of Dermatology · 1979 · 25 citations

Correlation between testicular tissue and H‐Y phenotype in intersex patients

U. Müller, A Mayerová, B. Debus et al. · Clinical Genetics · 1983 · 24 citations

Spermatogenesis, Histocompatibility, Fertility +19