Bibliographic Details
| Title: |
Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche. |
| Authors: |
Bizzarri C; Endocrinology Unit, Bambino Gesú Children's Hospital, IRCCS, P.zza S. Onofrio 4 00165, Rome, Italy. carla.bizzarri@opb.net, Crea F, Marini R, Benevento D, Porzio O, Ravà L, Cappa M |
| Source: |
Journal of pediatric endocrinology & metabolism : JPEM [J Pediatr Endocrinol Metab] 2012; Vol. 25 (11-12), pp. 1059-64. |
| Publication Type: |
Journal Article |
| Journal Info: |
Publisher: Walter de Gruyter Country of Publication: Germany NLM ID: 9508900 Publication Model: Print Cited Medium: Print ISSN: 0334-018X (Print) Linking ISSN: 0334018X NLM ISO Abbreviation: J Pediatr Endocrinol Metab Subsets: MEDLINE |
| Database: |
MEDLINE Ultimate |
