Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene

dc.creatorZECHI-CEIDEA, Roseli Maria
dc.creatorOLIVEIRA, Nelio Alessando Jesus
dc.creatorGUION-ALMEIDA, Maria Leine
dc.creatorANTUNES, Luis Fernando B. B.
dc.creatorRICHIERI-COSTA, Antonio
dc.creatorPASSOS-BUENO, Maria Rita Santos
dc.date.accessioned2012-10-20T02:03:25Z
dc.date.accessioned2018-07-04T15:29:21Z
dc.date.available2012-10-20T02:03:25Z
dc.date.available2018-07-04T15:29:21Z
dc.date.created2012-10-20T02:03:25Z
dc.date.issued2008
dc.identifierCLINICAL DYSMORPHOLOGY, v.17, n.3, p.225-226, 2008
dc.identifier0962-8827
dc.identifierhttp://producao.usp.br/handle/BDPI/26921
dc.identifierhttp://apps.isiknowledge.com/InboundService.do?Func=Frame&product=WOS&action=retrieve&SrcApp=EndNote&UT=000256891100018&Init=Yes&SrcAuth=ResearchSoft&mode=FullRecord
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1623571
dc.languageeng
dc.publisherLIPPINCOTT WILLIAMS & WILKINS
dc.relationClinical Dysmorphology
dc.rightsCopyright LIPPINCOTT WILLIAMS & WILKINS
dc.rightsclosedAccess
dc.titleUnusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene
dc.typeArtículos de revistas


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