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

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Title: Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome-An unexpected diagnosis of androgenetic chimera and its clinical implications.
Authors: Yu PT; Clinical Genetic Service, Department of Health, Hong Kong., Shu W; Department of Obstetrics and Gynaecology, Pamela Youde Nethersole Eastern Hospital, Hong Kong., Mok SL; Department of Obstetrics and Gynaecology, Princess Margaret Hospital, Hong Kong., Hui PW; Department of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong., Chan LW; Department of Obstetrics and Gynaecology, Pamela Youde Nethersole Eastern Hospital, Hong Kong., Kwok KY; Department of Obstetrics and Gynaecology, Prince of Wales Hospital, Hong Kong., Chan KYK; Prenatal Diagnostic Laboratory, Tsan Yuk Hospital, Hong Kong., Lo TK; Department of Obstetrics and Gynaecology, Princess Margaret Hospital, Hong Kong., Chung BHY; Department of Paediatrics & Adolescent Medicine, The University of Hong Kong, Hong Kong., Luk HM; Clinical Genetic Service, Department of Health, Hong Kong., Kan ASY; Department of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong.; Prenatal Diagnostic Laboratory, Tsan Yuk Hospital, Hong Kong.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2022 May; Vol. 188 (5), pp. 1562-1567. Date of Electronic Publication: 2022 Feb 18.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1552-4833
DOI:10.1002/ajmg.a.62665