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Article: Novel finding of lissencephaly and severe osteopenia in a Chinese patient with SATB2-associated syndrome and a brief review of literature

TitleNovel finding of lissencephaly and severe osteopenia in a Chinese patient with SATB2-associated syndrome and a brief review of literature
Authors
Lo, HYNg, WFFong, NCLui, CYDLam, CW
Issue Date2022
Citation
American Journal of Medical Genetics Part A, 2022 How to Cite?
DOI: http://dx.doi.org/10.1002/ajmg.a.62732
Persistent Identifierhttp://hdl.handle.net/10722/312703
ISI Accession Number ID
WOS:000771533400001

 

DC FieldValueLanguage
dc.contributor.authorLo, HY-
dc.contributor.authorNg, WF-
dc.contributor.authorFong, NC-
dc.contributor.authorLui, CYD-
dc.contributor.authorLam, CW-
dc.date.accessioned2022-05-12T10:54:26Z-
dc.date.available2022-05-12T10:54:26Z-
dc.date.issued2022-
dc.identifier.citationAmerican Journal of Medical Genetics Part A, 2022-
dc.identifier.urihttp://hdl.handle.net/10722/312703-
dc.languageeng-
dc.relation.ispartofAmerican Journal of Medical Genetics Part A-
dc.titleNovel finding of lissencephaly and severe osteopenia in a Chinese patient with SATB2-associated syndrome and a brief review of literature-
dc.typeArticle-
dc.identifier.emailLam, CW: ching-wanlam@pathology.hku.hk-
dc.identifier.authorityLam, CW=rp00260-
dc.identifier.doi10.1002/ajmg.a.62732-
dc.identifier.hkuros332922-
dc.identifier.isiWOS:000771533400001-

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