Mutations in MAGEL2 and L1CAM Are Associated With Congenital Hypopituitarism and Arthrogryposis

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dc.contributor.authorGregory, L.C.
dc.contributor.authorShah, P.
dc.contributor.authorSanner, J.R.F.
dc.contributor.authorArancibia, M.
dc.contributor.authorHurst, J.
dc.contributor.authorJones, W.D.
dc.contributor.authorSpoudeas, H.
dc.contributor.authorStabej, P.L.
dc.contributor.authorWilliams, H.J.
dc.contributor.authorOcaka, L.A.
dc.contributor.authorLoureiro Pérez, Carolina Andrea
dc.contributor.authorMartinez-Aguayo, A.
dc.contributor.authorDattani, M.T.
dc.date.accessioned2020-12-10T22:46:11Z
dc.date.available2020-12-10T22:46:11Z
dc.date.issued2019
dc.format.extent14 páginas
dc.fuente.origenConveris
dc.identifier.doi10.1210/jc.2019-00631
dc.identifier.issn0021-972X
dc.identifier.urihttps://doi.org/10.1210/jc.2019-00631
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/49892
dc.issue.numeroNo. 12
dc.language.isoen
dc.nota.accesoContenido completo
dc.pagina.final5750
dc.pagina.inicio5737
dc.revistaJournal of Clinical Endocrinology and Metabolismes_ES
dc.rightsacceso abierto
dc.titleMutations in MAGEL2 and L1CAM Are Associated With Congenital Hypopituitarism and Arthrogryposises_ES
dc.typeartículo
dc.volumenVol. 104
sipa.codpersvinculados199863
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