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Article: Analytical validity and clinical utility of whole-genome sequencing for cytogenetically balanced chromosomal abnormalities in prenatal diagnosis: abridged secondary publication

TitleAnalytical validity and clinical utility of whole-genome sequencing for cytogenetically balanced chromosomal abnormalities in prenatal diagnosis: abridged secondary publication
Authors
Chung, BHYKan, SYAChan, YKYang, WTang, HYMMak, CCY
Issue Date2022
Citation
Hong Kong Med J, 2022, v. 28 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/317424

 

DC FieldValueLanguage
dc.contributor.authorChung, BHY-
dc.contributor.authorKan, SYA-
dc.contributor.authorChan, YK-
dc.contributor.authorYang, W-
dc.contributor.authorTang, HYM-
dc.contributor.authorMak, CCY-
dc.date.accessioned2022-10-07T10:20:15Z-
dc.date.available2022-10-07T10:20:15Z-
dc.date.issued2022-
dc.identifier.citationHong Kong Med J, 2022, v. 28-
dc.identifier.urihttp://hdl.handle.net/10722/317424-
dc.languageeng-
dc.relation.ispartofHong Kong Med J-
dc.titleAnalytical validity and clinical utility of whole-genome sequencing for cytogenetically balanced chromosomal abnormalities in prenatal diagnosis: abridged secondary publication-
dc.typeArticle-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.emailYang, W: yangwl@hku.hk-
dc.identifier.emailTang, HYM: mhytang@hkucc.hku.hk-
dc.identifier.emailMak, CCY: cmakl@hku.hk-
dc.identifier.authorityChung, BHY=rp00473-
dc.identifier.authorityChan, YK=rp00453-
dc.identifier.authorityYang, W=rp00524-
dc.identifier.authorityTang, HYM=rp01701-
dc.identifier.hkuros338136-
dc.identifier.volume28-

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