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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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  Data: 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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  Data: <searchLink fieldCode="AU" term="%22Yu+PT%22">Yu PT</searchLink>; Clinical Genetic Service, Department of Health, Hong Kong.<br /><searchLink fieldCode="AU" term="%22Shu+W%22">Shu W</searchLink>; Department of Obstetrics and Gynaecology, Pamela Youde Nethersole Eastern Hospital, Hong Kong.<br /><searchLink fieldCode="AU" term="%22Mok+SL%22">Mok SL</searchLink>; Department of Obstetrics and Gynaecology, Princess Margaret Hospital, Hong Kong.<br /><searchLink fieldCode="AU" term="%22Hui+PW%22">Hui PW</searchLink>; Department of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong.<br /><searchLink fieldCode="AU" term="%22Chan+LW%22">Chan LW</searchLink>; Department of Obstetrics and Gynaecology, Pamela Youde Nethersole Eastern Hospital, Hong Kong.<br /><searchLink fieldCode="AU" term="%22Kwok+KY%22">Kwok KY</searchLink>; Department of Obstetrics and Gynaecology, Prince of Wales Hospital, Hong Kong.<br /><searchLink fieldCode="AU" term="%22Chan+KYK%22">Chan KYK</searchLink>; Prenatal Diagnostic Laboratory, Tsan Yuk Hospital, Hong Kong.<br /><searchLink fieldCode="AU" term="%22Lo+TK%22">Lo TK</searchLink>; Department of Obstetrics and Gynaecology, Princess Margaret Hospital, Hong Kong.<br /><searchLink fieldCode="AU" term="%22Chung+BHY%22">Chung BHY</searchLink>; Department of Paediatrics & Adolescent Medicine, The University of Hong Kong, Hong Kong.<br /><searchLink fieldCode="AU" term="%22Luk+HM%22">Luk HM</searchLink>; Clinical Genetic Service, Department of Health, Hong Kong.<br /><searchLink fieldCode="AU" term="%22Kan+ASY%22">Kan ASY</searchLink>; Department of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong.; Prenatal Diagnostic Laboratory, Tsan Yuk Hospital, Hong Kong.
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  Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2022 May; Vol. 188 (5), pp. 1562-1567. <i>Date of Electronic Publication: </i>2022 Feb 18.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101235741 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1552-4833 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524825%22">15524825 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet A <i>Subsets: </i>MEDLINE
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        Value: 10.1002/ajmg.a.62665
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        Text: English
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        StartPage: 1562
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      – TitleFull: 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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              M: 05
              Text: 2022 May
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            – TitleFull: American journal of medical genetics. Part A
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