A deletion of more than 800 kb is the most recurrent mutation in chilean patients with SHOX gene defects

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dc.contributor.authorPoggi, Helena
dc.contributor.authorVera, A.
dc.contributor.authorAvalos, C.
dc.contributor.authorLagos, M.
dc.contributor.authorMellado Sagredo, Cecilia
dc.contributor.authorAracena Álvarez, Mariana Inés
dc.contributor.authorAravena, T.
dc.contributor.authorGarcía Bruce, Hernán
dc.contributor.authorGodoy Cortés, Claudia Loreto
dc.contributor.authorCattani Ortega, Andreina
dc.contributor.authorReyes, L.
dc.contributor.authorLacourt, P.
dc.contributor.authorRumié Carmi, Hana K.
dc.contributor.authorMericq, V.
dc.contributor.authorArriaza, M.
dc.contributor.authorMartinez-Aguayo, A.
dc.date.accessioned2020-08-21T17:15:19Z
dc.date.available2020-08-21T17:15:19Z
dc.date.issued2015
dc.format.extent4 páginas
dc.fuente.origenConveris
dc.identifier.doi10.1159/000439109
dc.identifier.issn1663-2818
dc.identifier.issn1663-2826
dc.identifier.urihttps://doi.org/10.1159/000439109
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/39177
dc.issue.numeroNo. 4
dc.language.isoen
dc.pagina.final257
dc.pagina.inicio254
dc.revistaHormone Research in Paediatricses_ES
dc.rightsacceso restringido
dc.subject.ddc610
dc.subject.deweyMedicina y saludes_ES
dc.subject.otherDisplasiaes_ES
dc.subject.otherfibrosa óseaes_ES
dc.subject.otherEstaturaes_ES
dc.titleA deletion of more than 800 kb is the most recurrent mutation in chilean patients with SHOX gene defectses_ES
dc.typeartículo
dc.volumenVol. 84
sipa.codpersvinculados1002671
sipa.codpersvinculados99831
sipa.codpersvinculados1006495
sipa.codpersvinculados69895
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