Genetic Evidence of the Association of DEAH-Box Helicase 37 Defects With 46,XY Gonadal Dysgenesis Spectrum

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dc.contributor.authorDa Silva, T.E.
dc.contributor.authorGomes, N.L.
dc.contributor.authorLerario, A.M.
dc.contributor.authorKeegan, C.E.
dc.contributor.authorNishi, M.Y.
dc.contributor.authorCarvalho, F.M.
dc.contributor.authorVilain, E.
dc.contributor.authorBarseghyan, H.
dc.contributor.authorMartínez Aguayo, Alejandro Gregorio
dc.contributor.authorForclaz, M.V.
dc.contributor.authorPapazian, R.
dc.contributor.authorDe Paula, L.C.P.
dc.contributor.authorCosta, E.C.
dc.contributor.authorCarvalho, L.R.
dc.contributor.authorLima Jorge, A.A.
dc.contributor.authorMartins Elias, F.
dc.contributor.authorMitchell, R.
dc.contributor.authorFrade Costa, E.M.
dc.contributor.authorBilharinho Mendonca, B.
dc.contributor.authorDomenice, S.
dc.date.accessioned2020-11-25T17:31:29Z
dc.date.available2020-11-25T17:31:29Z
dc.date.issued2019
dc.format.extent12 páginas
dc.fuente.origenConveris
dc.identifier.doi10.1210/jc.2019-00984
dc.identifier.issn0021-972X
dc.identifier.urihttps://doi.org/10.1210/jc.2019-00984
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/48567
dc.issue.numeroNo. 12
dc.language.isoen
dc.nota.accesoContenido completo
dc.pagina.final5934
dc.pagina.inicio5923
dc.revistaJournal of Clinical Endocrinology and Metabolismes_ES
dc.rightsacceso abierto
dc.titleGenetic Evidence of the Association of DEAH-Box Helicase 37 Defects With 46,XY Gonadal Dysgenesis Spectrumes_ES
dc.typeartículo
dc.volumenVol. 104
sipa.codpersvinculados1003862
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