Please use this identifier to cite or link to this item: http://repositorio.unitau.br/jspui/handle/20.500.11874/3267
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dc.contributor.authorHart, Patricia Suzannept_BR
dc.contributor.authorPallos, Déborapt_BR
dc.contributor.authorCortelli, José Robertopt_BR
dc.contributor.authorVain, Spt_BR
dc.contributor.authorWright, JTpt_BR
dc.contributor.authorKorkko, Jpt_BR
dc.contributor.authorHart, Thomas Charlespt_BR
dc.date.accessioned2019-09-12T16:57:21Z-
dc.date.available2019-09-12T16:57:21Z-
dc.date.issued2000-
dc.citation.volume67pt_BR
dc.citation.issue4pt_BR
dc.citation.spage387-
dc.citation.epage387-
dc.identifier.issn0002-9297-
dc.identifier.urihttp://repositorio.unitau.br/jspui/handle/20.500.11874/3267-
dc.descriptionSuplemento (2)pt_BR
dc.description.provenanceMade available in DSpace on 2019-09-12T16:57:21Z (GMT). No. of bitstreams: 0 Previous issue date: 2000en
dc.languageInglêspt_BR
dc.publisherUniv Chicago Press-
dc.publisher.countryEstados Unidospt_BR
dc.relation.ispartofAmerican Journal of Human Genetics-
dc.rightsEm verificaçãopt_BR
dc.sourceWeb of Sciencept_BR
dc.titleNovel COL1A1 mutation (G599C) associated with mild osteogenesis imperfecta and dentinogenesis imperfecta.en
dc.typeResumopt_BR
dc.identifier.wosWOS:000089400702170-
dc.description.affiliationUniv Pittsburgh, Pittsburgh, PA USA; Universidade de Taubaté (Unitau), Sao Paulo, Brazil; Univ N Carolina, Chapel Hill, NC USA; Med Coll Penn & Hahnemann Univ, Ctr Gene Therapy, Philadelphia, PA USA-
dc.subject.wosareaGenetics & Heredityen
dc.subject.researchareaGenetics & Heredityen
Appears in Collections:Artigos de Periódicos

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