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Low-pass genome sequencing-based detection of absence of heterozygosity: validation in clinical cytogenetics.
Dong, Zirui; Chau, Matthew Hoi Kin; Zhang, Yanyan; Yang, Zhenjun; Shi, Mengmeng; Wah, Yi Man; Kwok, Yvonne K; Leung, Tak Yeung; Morton, Cynthia C; Choy, Kwong Wai.
Afiliação
  • Dong Z; Department of Obstetrics & Gynaecology, The Chinese University of Hong Kong, Hong Kong, China.
  • Chau MHK; Key Laboratory for Regenerative Medicine, Ministry of Education (Shenzhen Base), Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China.
  • Zhang Y; Hong Kong Hub of Paediatric Excellence, The Chinese University of Hong Kong, Hong Kong, China.
  • Yang Z; Department of Obstetrics & Gynaecology, The Chinese University of Hong Kong, Hong Kong, China.
  • Shi M; Key Laboratory for Regenerative Medicine, Ministry of Education (Shenzhen Base), Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China.
  • Wah YM; Hong Kong Hub of Paediatric Excellence, The Chinese University of Hong Kong, Hong Kong, China.
  • Kwok YK; Department of Obstetrics & Gynaecology, The Chinese University of Hong Kong, Hong Kong, China.
  • Leung TY; Department of Obstetrics & Gynaecology, The Chinese University of Hong Kong, Hong Kong, China.
  • Morton CC; Key Laboratory for Regenerative Medicine, Ministry of Education (Shenzhen Base), Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China.
  • Choy KW; Department of Obstetrics & Gynaecology, The Chinese University of Hong Kong, Hong Kong, China.
Genet Med ; 23(7): 1225-1233, 2021 07.
Article em En | MEDLINE | ID: mdl-33772221
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Dissomia Uniparental Tipo de estudo: Diagnostic_studies / Guideline Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Dissomia Uniparental Tipo de estudo: Diagnostic_studies / Guideline Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article