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Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental Disorders.
Cao, Ye; Luk, Ho Ming; Zhang, Yanyan; Chau, Matthew Hoi Kin; Xue, Shuwen; Cheng, Shirley S W; Li, Albert Martin; Chong, Josephine S C; Leung, Tak Yeung; Dong, Zirui; Choy, Kwong Wai; Lo, Ivan Fai Man.
Afiliação
  • Cao Y; Department of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Luk HM; Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Zhang Y; Key Laboratory for Regenerative Medicine, Ministry of Education (Shenzhen Base), Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China.
  • Chau MHK; Hong Kong Hub of Paediatric Excellence, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Xue S; Clinical Genetic Service, Department of Health, Hong Kong SAR, China.
  • Cheng SSW; Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Li AM; Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Chong JSC; Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Leung TY; Clinical Genetic Service, Department of Health, Hong Kong SAR, China.
  • Dong Z; Department of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Choy KW; Hong Kong Hub of Paediatric Excellence, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Lo IFM; Department of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.
Front Genet ; 13: 803088, 2022.
Article em En | MEDLINE | ID: mdl-35495136

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article