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Article: Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications

TitlePrenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications
Authors
Yu, PTShu, WMok, SLHui, PWChan, LWKwok, KYChan, YKLo, TKChung, BHYLuk, HMKan, SYA
Issue Date2022
Citation
American Journal of Medical Genetics Part A, 2022 How to Cite?
DOI: http://dx.doi.org/10.1002/ajmg.a.62665
Persistent Identifierhttp://hdl.handle.net/10722/311184
ISI Accession Number ID
WOS:000757420500001

 

DC FieldValueLanguage
dc.contributor.authorYu, PT-
dc.contributor.authorShu, W-
dc.contributor.authorMok, SL-
dc.contributor.authorHui, PW-
dc.contributor.authorChan, LW-
dc.contributor.authorKwok, KY-
dc.contributor.authorChan, YK-
dc.contributor.authorLo, TK-
dc.contributor.authorChung, BHY-
dc.contributor.authorLuk, HM-
dc.contributor.authorKan, SYA-
dc.date.accessioned2022-03-04T12:53:41Z-
dc.date.available2022-03-04T12:53:41Z-
dc.date.issued2022-
dc.identifier.citationAmerican Journal of Medical Genetics Part A, 2022-
dc.identifier.urihttp://hdl.handle.net/10722/311184-
dc.languageeng-
dc.relation.ispartofAmerican Journal of Medical Genetics Part A-
dc.titlePrenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications-
dc.typeArticle-
dc.identifier.emailChan, YK: ykchanc@hku.hk-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.authorityChan, YK=rp00453-
dc.identifier.authorityChung, BHY=rp00473-
dc.identifier.doi10.1002/ajmg.a.62665-
dc.identifier.hkuros332031-
dc.identifier.isiWOS:000757420500001-

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