Your browser doesn't support javascript.
loading
Correlation between genotype and hormonal levels in heterozygous mutation carriers and non-carriers of 21-hydroxylase deficiency.
Napolitano, E; Manieri, C; Restivo, F; Composto, E; Lanfranco, F; Repici, M; Pasini, B; Einaudi, S; Menegatti, E.
Affiliation
  • Napolitano E; Division of Endocrinology, Diabetology and Metabolism, Department of Internal Medicine, University of Turin, Turin, Italy.
J Endocrinol Invest ; 34(7): 498-501, 2011.
Article in En | MEDLINE | ID: mdl-20671415
Subject(s)
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Steroid 21-Hydroxylase / Carrier State / Adrenal Hyperplasia, Congenital / 17-alpha-Hydroxyprogesterone / Genotype / Mutation Type of study: Diagnostic_studies Limits: Female / Humans / Male Language: En Journal: J Endocrinol Invest Year: 2011 Document type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Steroid 21-Hydroxylase / Carrier State / Adrenal Hyperplasia, Congenital / 17-alpha-Hydroxyprogesterone / Genotype / Mutation Type of study: Diagnostic_studies Limits: Female / Humans / Male Language: En Journal: J Endocrinol Invest Year: 2011 Document type: Article