Six Additional Cases Of Sedc Due To The Same And Recurrent R989c Mutation In The Col2a1 Gene-the Clinical And Radiological Follow-up.

dc.creatorC Silveira, Karina
dc.creatorC Bonadia, Luciana
dc.creatorSuperti-Furga, Andrea
dc.creatorR Bertola, Débora
dc.creatorA L Jorge, Alexander
dc.creatorP Cavalcanti, Denise
dc.date2015-Mar
dc.date2015-11-27T13:46:19Z
dc.date2015-11-27T13:46:19Z
dc.date.accessioned2018-03-29T01:23:44Z
dc.date.available2018-03-29T01:23:44Z
dc.identifierAmerican Journal Of Medical Genetics. Part A. , 2015-Mar.
dc.identifier1552-4833
dc.identifier10.1002/ajmg.a.36954
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/25735649
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/202177
dc.identifier25735649
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1302410
dc.description
dc.description
dc.description
dc.languageeng
dc.relationAmerican Journal Of Medical Genetics. Part A
dc.relationAm. J. Med. Genet. A
dc.rightsfechado
dc.rights
dc.sourcePubMed
dc.titleSix Additional Cases Of Sedc Due To The Same And Recurrent R989c Mutation In The Col2a1 Gene-the Clinical And Radiological Follow-up.
dc.typeCarta


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