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CTNNB1-related neurodevelopmental disorder in a Chinese population: A case series.
Ho, Stephanie; Tsang, Mandy Ho-Yin; Fung, Jasmine Lee-Fong; Huang, Haibo; Chow, Chun-Bong; Cheng, Shirley Sze-Wing; Luk, Ho-Ming; Chung, Brian Hon-Yin; Lo, Ivan Fai-Man.
Afiliação
  • Ho S; Clinical Genetic Service, Department of Health, Hong Kong, China.
  • Tsang MH; Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Fung JL; Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Huang H; Department of Pediatrics, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
  • Chow CB; Department of Pediatrics, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
  • Cheng SS; Clinical Genetic Service, Department of Health, Hong Kong, China.
  • Luk HM; Clinical Genetic Service, Department of Health, Hong Kong, China.
  • Chung BH; Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Lo IF; Clinical Genetic Service, Department of Health, Hong Kong, China.
Am J Med Genet A ; 188(1): 130-137, 2022 01.
Article em En | MEDLINE | ID: mdl-34558805
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos do Neurodesenvolvimento / Microcefalia Tipo de estudo: Diagnostic_studies Limite: Humans País como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos do Neurodesenvolvimento / Microcefalia Tipo de estudo: Diagnostic_studies Limite: Humans País como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article