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Article: De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients

TitleDe novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients
Authors
Issue Date2016
PublisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/npjgenmed/
Citation
npj Genomic Medicine, 2016, v. 1, p. 16033:1-8 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/238684
ISSN
2023 Impact Factor: 4.7
2023 SCImago Journal Rankings: 2.105
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorMAK, CCY-
dc.contributor.authorChow, PC-
dc.contributor.authorLiu, APY-
dc.contributor.authorChan, YK-
dc.contributor.authorChu, WY-
dc.contributor.authorMok, TKG-
dc.contributor.authorLEUNG, KC-
dc.contributor.authorYEUNG, KS-
dc.contributor.authorChau, AKT-
dc.contributor.authorLowther, C-
dc.contributor.authorScherer, SW-
dc.contributor.authorMarshall, CR-
dc.contributor.authorBassett, AS-
dc.contributor.authorChung, BHY-
dc.date.accessioned2017-02-20T01:24:44Z-
dc.date.available2017-02-20T01:24:44Z-
dc.date.issued2016-
dc.identifier.citationnpj Genomic Medicine, 2016, v. 1, p. 16033:1-8-
dc.identifier.issn2056-7944-
dc.identifier.urihttp://hdl.handle.net/10722/238684-
dc.languageeng-
dc.publisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/npjgenmed/-
dc.relation.ispartofnpj Genomic Medicine-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleDe novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients-
dc.typeArticle-
dc.identifier.emailLiu, APY: apyliu@hku.hk-
dc.identifier.emailChan, YK: ykchanc@hku.hk-
dc.identifier.emailChu, WY: chuwyy@hku.hk-
dc.identifier.emailMok, TKG: gtkmok@hku.hk-
dc.identifier.emailChau, AKT: aktchau@hku.hk-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.authorityLiu, APY=rp01357-
dc.identifier.authorityChan, YK=rp00453-
dc.identifier.authorityChung, BHY=rp00473-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/npjgenmed.2016.33-
dc.identifier.scopuseid_2-s2.0-85021334603-
dc.identifier.hkuros271407-
dc.identifier.volume1-
dc.identifier.spage16033:1-
dc.identifier.epage8-
dc.identifier.isiWOS:000413238400001-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl2056-7944-

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