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Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia.
Barbaro, M; Lajic, S; Baldazzi, L; Balsamo, A; Pirazzoli, P; Cicognani, A; Wedell, A; Cacciari, E.
Affiliation
  • Barbaro M; Department of Pediatrics, University of Bologna and S. Orsola-Malpighi Hospital, 40139 Bologna, Italy. michael.barbaro@cmm.ki.se
J Clin Endocrinol Metab ; 89(5): 2402-7, 2004 May.
Article in En | MEDLINE | ID: mdl-15126570
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Steroid 21-Hydroxylase / Adrenal Hyperplasia, Congenital Type of study: Prognostic_studies Limits: Adolescent / Animals / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Country/Region as subject: Europa Language: En Journal: J Clin Endocrinol Metab Year: 2004 Document type: Article Affiliation country:
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Steroid 21-Hydroxylase / Adrenal Hyperplasia, Congenital Type of study: Prognostic_studies Limits: Adolescent / Animals / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Country/Region as subject: Europa Language: En Journal: J Clin Endocrinol Metab Year: 2004 Document type: Article Affiliation country: