Your browser doesn't support javascript.
loading
17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations.
Boehmer, A L; Brinkmann, A O; Sandkuijl, L A; Halley, D J; Niermeijer, M F; Andersson, S; de Jong, F H; Kayserili, H; de Vroede, M A; Otten, B J; Rouwé, C W; Mendonça, B B; Rodrigues, C; Bode, H H; de Ruiter, P E; Delemarre-van de Waal, H A; Drop, S L.
Affiliation
  • Boehmer AL; Department of Pediatrics, Sophia Children's Hospital, Rotterdam, The Netherlands. boehmer@ALKG.AZR.NL
J Clin Endocrinol Metab ; 84(12): 4713-21, 1999 Dec.
Article in En | MEDLINE | ID: mdl-10599740
Subject(s)
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Genetics, Population / 17-Hydroxysteroid Dehydrogenases Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans / Male Country/Region as subject: Europa Language: En Journal: J Clin Endocrinol Metab Year: 1999 Document type: Article Affiliation country: Netherlands Country of publication: United States
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Genetics, Population / 17-Hydroxysteroid Dehydrogenases Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans / Male Country/Region as subject: Europa Language: En Journal: J Clin Endocrinol Metab Year: 1999 Document type: Article Affiliation country: Netherlands Country of publication: United States