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Article: Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care

TitleUnder-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care
Authors
Liu, APYChow, PCLee, PPWMok, GTKTang, WFLau, ETKLam, STSChan, YKKan, SYAChau, AKTCheung, YFLau, YLChung, BHY
Keywords22q11.2 deletion syndrome (22q11.2DS)
Adult
Chinese
Congenital heart disease
Conotruncal anomaly
Dysmorphism
Issue Date2014
PublisherElsevier France, Editions Scientifiques et Medicales. The Journal's web site is located at http://www.elsevier.com/locate/ejmg
Citation
European Journal of Medical Genetics, 2014, v. 57 n. 6, p. 306-311 How to Cite?
DOI: http://dx.doi.org/10.1016/j.ejmg.2014.03.014
Persistent Identifierhttp://hdl.handle.net/10722/196796
ISSN
1769-7212
2023 Impact Factor: 1.6
2023 SCImago Journal Rankings: 0.666
ISI Accession Number ID
WOS:000336402300014

 

DC FieldValueLanguage
dc.contributor.authorLiu, APY-
dc.contributor.authorChow, PC-
dc.contributor.authorLee, PPW-
dc.contributor.authorMok, GTK-
dc.contributor.authorTang, WF-
dc.contributor.authorLau, ETK-
dc.contributor.authorLam, STS-
dc.contributor.authorChan, YK-
dc.contributor.authorKan, SYA-
dc.contributor.authorChau, AKT-
dc.contributor.authorCheung, YF-
dc.contributor.authorLau, YL-
dc.contributor.authorChung, BHY-
dc.date.accessioned2014-04-29T03:41:58Z-
dc.date.available2014-04-29T03:41:58Z-
dc.date.issued2014-
dc.identifier.citationEuropean Journal of Medical Genetics, 2014, v. 57 n. 6, p. 306-311-
dc.identifier.issn1769-7212-
dc.identifier.urihttp://hdl.handle.net/10722/196796-
dc.languageeng-
dc.publisherElsevier France, Editions Scientifiques et Medicales. The Journal's web site is located at http://www.elsevier.com/locate/ejmg-
dc.relation.ispartofEuropean Journal of Medical Genetics-
dc.rightsNOTICE: this is the author’s version of a work that was accepted for publication in <Journal title>. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in PUBLICATION, [VOL#, ISSUE#, (DATE)] DOI#en_US
dc.subject22q11.2 deletion syndrome (22q11.2DS)-
dc.subjectAdult-
dc.subjectChinese-
dc.subjectCongenital heart disease-
dc.subjectConotruncal anomaly-
dc.subjectDysmorphism-
dc.titleUnder-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care-
dc.typeArticle-
dc.identifier.emailLiu, APY: apyliu@hku.hk-
dc.identifier.emailLee, PPW: ppwlee@hku.hk-
dc.identifier.emailMok, GTK: gtkmok@hku.hk-
dc.identifier.emailTang, WF: h9705682@graduate.hku.hk-
dc.identifier.emailLau, ETK: etklau@hkucc.hku.hk-
dc.identifier.emailChan, YK: ykchanc@hku.hk-
dc.identifier.emailKan, SYA: kansya@hku.hk-
dc.identifier.emailChau, AKT: aktchau@hku.hk-
dc.identifier.emailCheung, YF: xfcheung@hku.hk-
dc.identifier.emailLau, YL: lauylung@hku.hk-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.authorityLiu, APY=rp01357-
dc.identifier.authorityLee, PPW=rp00462-
dc.identifier.authorityChan, YK=rp00453-
dc.identifier.authorityCheung, YF=rp00382-
dc.identifier.authorityLau, YL=rp00361-
dc.identifier.authorityChung, BHY=rp00473-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.ejmg.2014.03.014-
dc.identifier.pmid24721633-
dc.identifier.scopuseid_2-s2.0-84901024217-
dc.identifier.hkuros228674-
dc.identifier.volume57-
dc.identifier.issue6-
dc.identifier.spage306-
dc.identifier.epage311-
dc.identifier.isiWOS:000336402300014-
dc.publisher.placeFrance-
dc.identifier.issnl1769-7212-

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