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Article: Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability

DC FieldValueLanguage
dc.contributor.authorTan, NB-
dc.contributor.authorPagnamenta, AT-
dc.contributor.authorFerla, MP-
dc.contributor.authorGadian, J-
dc.contributor.authorChung, BHY-
dc.contributor.authorChan, MCY-
dc.contributor.authorFung, LF-
dc.contributor.authorCook, E-
dc.contributor.authorGuter, S-
dc.contributor.authorBoschann, F-
dc.contributor.authorHeinen, A-
dc.contributor.authorSchallne, J-
dc.contributor.authorMignot, C-
dc.contributor.authorKeren, B-
dc.contributor.authorWhalen, S-
dc.contributor.authorSarret, C-
dc.contributor.authorMittag, D-
dc.contributor.authorDemmer, L-
dc.contributor.authorStapleton, R-
dc.contributor.authorSaida, K-
dc.contributor.authorMatsumoto, N-
dc.contributor.authorMiyake, N-
dc.contributor.authorSheffer, R-
dc.contributor.authorMor-Shaked, H-
dc.contributor.authorBarnett, CP-
dc.contributor.authorByrne, AB-
dc.contributor.authorScott, HS-
dc.contributor.authorKraus, A-
dc.contributor.authorCappuccio, G-
dc.contributor.authorBrunetti-Pierri, N-
dc.contributor.authorIorio, R-
dc.contributor.authorDi Dato, F-
dc.contributor.authorPais, LS-
dc.contributor.authorYeung, A-
dc.contributor.authorTan, TY-
dc.contributor.authorTaylor, JC-
dc.contributor.authorChristodoulou, J-
dc.contributor.authorWhite, S-
dc.date.accessioned2021-07-27T08:08:47Z-
dc.date.available2021-07-27T08:08:47Z-
dc.date.issued2021-
dc.identifier.citationJournal of Medical Genetics, 2021, p. jmedgenet-2020-107462-
dc.identifier.urihttp://hdl.handle.net/10722/301280-
dc.languageeng-
dc.relation.ispartofJournal of Medical Genetics-
dc.titleRecurrent de novo missense variants in GNB2 can cause syndromic intellectual disability -
dc.typeArticle-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.emailTan, TY: tanty@hku.hk-
dc.identifier.authorityChung, BHY=rp00473-
dc.identifier.authorityTan, TY=rp01380-
dc.identifier.doi10.1136/jmedgenet-2020-107462-
dc.identifier.scopuseid_2-s2.0-85108959165-
dc.identifier.hkuros323673-
dc.identifier.spagejmedgenet-
dc.identifier.epage2020-
dc.identifier.isiWOS:000725016200001-

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