z-logo
open-access-imgOpen Access
High Incidence of Molecular Defects of the CYP21 Gene in Patients with Premature Adrenarche
Author(s) -
C. Dacou-Voutetakis
Publication year - 1999
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.84.5.1570
Subject(s) - adrenarche , medicine , endocrinology , virilization , genotype , allele , bone age , compound heterozygosity , androstenedione , dehydroepiandrosterone sulfate , biology , hormone , genetics , gene , androgen

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom