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Article: Phenotypic spectrum associated with PTCHD1 deletion and truncating mutations includes intellectual disability and autism spectrum disorder

DC FieldValueLanguage
dc.contributor.authorChaudhry, Aen_US
dc.contributor.authorNoor, Aen_US
dc.contributor.authorDegagne, Ben_US
dc.contributor.authorBaker, Ken_US
dc.contributor.authorBok, LAen_US
dc.contributor.authorBrady, AFen_US
dc.contributor.authorChitayat, Den_US
dc.contributor.authorChung, BHYen_US
dc.contributor.authorCytrynbaum, Cen_US
dc.contributor.authorDyment, Den_US
dc.contributor.authorFilges, Ien_US
dc.contributor.authorHelm, Ben_US
dc.contributor.authorHutchison, HTen_US
dc.contributor.authorJeng, LJBen_US
dc.contributor.authorLaumonnier, Fen_US
dc.contributor.authorMarshall, CRen_US
dc.contributor.authorMenzel, Men_US
dc.contributor.authorParkash, Sen_US
dc.contributor.authorParker, MJen_US
dc.contributor.authorThe, DDD STUDYen_US
dc.contributor.authorRaymond, FLen_US
dc.contributor.authorRideout, ALen_US
dc.contributor.authorRoberts, Wen_US
dc.contributor.authorRupps, Ren_US
dc.contributor.authorSchanze, Ien_US
dc.contributor.authorSchrander-Stumpel, CTRMen_US
dc.contributor.authorSpeevak, MDen_US
dc.contributor.authorStavropoulos, DJen_US
dc.contributor.authorStevens, SJCen_US
dc.contributor.authorThomas, ERAen_US
dc.contributor.authorToutain, Aen_US
dc.contributor.authorVergano, Sen_US
dc.contributor.authorWeksberg, Ren_US
dc.contributor.authorScherer, SWen_US
dc.contributor.authorVincent, JBen_US
dc.contributor.authorCarter, MTen_US
dc.date.accessioned2014-09-19T13:51:21Z-
dc.date.available2014-09-19T13:51:21Z-
dc.date.issued2015-
dc.identifier.citationClinical Genetics (In press), 2015en_US
dc.identifier.urihttp://hdl.handle.net/10722/203278-
dc.languageengen_US
dc.relation.ispartofClinical Geneticsen_US
dc.titlePhenotypic spectrum associated with PTCHD1 deletion and truncating mutations includes intellectual disability and autism spectrum disorderen_US
dc.typeArticleen_US
dc.identifier.emailChung, BHY: bhychung@hku.hken_US
dc.identifier.authorityChung, BHY=rp00473en_US
dc.identifier.doi10.1111/cge.12482en_US
dc.identifier.hkuros237547en_US

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