Clinical features of chromosome 22q11.2 microdeletion syndrome in 208 chilean patients

CLINICAL GENETICS;
CLIN GENET

dc.creatorRepetto, G. M.
dc.creatorGuzman, M. L.
dc.creatorPuga, A.
dc.creatorCalderon, J. F.
dc.creatorAstete, C. P.
dc.creatorAracena, M.
dc.creatorArriaza, M.
dc.creatorAravena, T.
dc.creatorSanz, P.
dc.date2016-12-01T21:38:40Z
dc.date2022-07-06T15:59:16Z
dc.date2016-12-01T21:38:40Z
dc.date2022-07-06T15:59:16Z
dc.date2009
dc.date.accessioned2023-08-21T22:27:23Z
dc.date.available2023-08-21T22:27:23Z
dc.identifier1061051
dc.identifier1061051
dc.identifier0009-9163
dc.identifierhttps://hdl.handle.net/10533/136710
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8290077
dc.description11
dc.descriptionFONDECYT
dc.description5
dc.descriptionFONDECYT
dc.description76
dc.languageeng
dc.publisherMUNKSGAARD
dc.relationinstname: Conicyt
dc.relationreponame: Repositorio Digital RI2.0
dc.relationinstname: Conicyt
dc.relationreponame: Repositorio Digital RI2.0
dc.relationinfo:eu-repo/grantAgreement/Fondecyt/1061051
dc.relationinfo:eu-repo/semantics/dataset/hdl.handle.net/10533/93477
dc.relationhttps://doi.org/10.1111/j.1399-0004.2009.01234.x
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleClinical features of chromosome 22q11.2 microdeletion syndrome in 208 chilean patients
dc.titleCLINICAL GENETICS
dc.titleCLIN GENET
dc.typeArticulo
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.coverageHOBOKEN


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