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Article: A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report

TitleA Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report
Authors
Ng, KSVLau, TKKan, SYAChung, BHYLuk, HMNg, WFShi, MChoy, KWCao, YLeung, WC
Issue Date2021
Citation
Diagnostics, 2021, v. 11, p. 1576 How to Cite?
DOI: http://dx.doi.org/10.3390/diagnostics11091576
Persistent Identifierhttp://hdl.handle.net/10722/313536
ISI Accession Number ID
WOS:000699088600001

 

DC FieldValueLanguage
dc.contributor.authorNg, KSV-
dc.contributor.authorLau, TK-
dc.contributor.authorKan, SYA-
dc.contributor.authorChung, BHY-
dc.contributor.authorLuk, HM-
dc.contributor.authorNg, WF-
dc.contributor.authorShi, M-
dc.contributor.authorChoy, KW-
dc.contributor.authorCao, Y-
dc.contributor.authorLeung, WC-
dc.date.accessioned2022-06-17T06:47:51Z-
dc.date.available2022-06-17T06:47:51Z-
dc.date.issued2021-
dc.identifier.citationDiagnostics, 2021, v. 11, p. 1576-
dc.identifier.urihttp://hdl.handle.net/10722/313536-
dc.languageeng-
dc.relation.ispartofDiagnostics-
dc.titleA Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report-
dc.typeArticle-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.emailLeung, WC: leungwc6@hkucc.hku.hk-
dc.identifier.authorityChung, BHY=rp00473-
dc.identifier.doi10.3390/diagnostics11091576-
dc.identifier.hkuros333424-
dc.identifier.volume11-
dc.identifier.spage1576-
dc.identifier.epage1576-
dc.identifier.isiWOS:000699088600001-

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