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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.
Yu, Pui-Tak; Shu, Wendy; Mok, Sau-Lan; Hui, Pui-Wah; Chan, Lin-Wai; Kwok, Ka-Yin; Chan, Kelvin Y K; Lo, Tsz-Kin; Chung, Brian H Y; Luk, Ho-Ming; Kan, Anita S Y.
Afiliação
  • 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.
Am J Med Genet A ; 188(5): 1562-1567, 2022 05.
Article em En | MEDLINE | ID: mdl-35179302
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Beckwith-Wiedemann Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article