Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/328100
Type: Resumo
Title: A Novel Cyp21a2 Mutation Identified A Patient With Classical 21-hydroxylase Deficiency
Author: Michelato
Dd P.; Petroli
R. J.; Santos
L. Gd; Monlleo
I. L.; Mello
M. Pd
Editor: Karger
Basel
Citation: Hormone Research In Paediatrics. Karger, v. 86, p. 75 - 75, 2016.
Rights: fechado
Identifier DOI: 10.1159/000451040
Address: https://www.karger.com/Journal/Issue/273140
Date Issue: 2016
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File SizeFormat 
000388504100157.pdf604.81 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.