Analytical validity and clinical utility of whole-genome sequencing for cytogenetically balanced chromosomal abnormalities in prenatal diagnosis: abridged secondary publication.

Chung, B H Y; Kan, A S Y; Chan, K Y K; Yang, W; Tang, M H Y; Mak, C C Y; Leung, G K C

Chung, B H Y; Kan, A S Y; Chan, K Y K; Yang, W; Tang, M H Y; Mak, C C Y; Leung, G K C.

Afiliação

Chung BHY; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong.
Kan ASY; Department of Obstetrics and Gynaecology, Queen Mary Hospital, The University of Hong Kong.
Chan KYK; Department of Obstetrics and Gynaecology, Queen Mary Hospital, The University of Hong Kong.
Yang W; Prenatal Diagnostic Laboratory, Department of Obstetrics and Gynaecology, Tsan Yuk Hospital.
Tang MHY; Department of Obstetrics and Gynaecology, Queen Mary Hospital, The University of Hong Kong.
Mak CCY; Prenatal Diagnostic Laboratory, Department of Obstetrics and Gynaecology, Tsan Yuk Hospital.
Leung GKC; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong.

Hong Kong Med J ; 28 Suppl 1(1): 4-7, 2022 02.

Article em En | MEDLINE | ID: mdl-35260506

Assuntos

Aberrações Cromossômicas; Diagnóstico Pré-Natal; Feminino; Humanos; Gravidez; Sequenciamento Completo do Genoma

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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Aberrações Cromossômicas Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Pregnancy Idioma: En Revista: Hong Kong Med J Assunto da revista: MEDICINA Ano de publicação: 2022 Tipo de documento: Article

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