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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.
Afiliación
  • 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 en En | MEDLINE | ID: mdl-34558805
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trastornos del Neurodesarrollo / Microcefalia Tipo de estudio: Diagnostic_studies País/Región como asunto: Asia Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Trastornos del Neurodesarrollo / Microcefalia Tipo de estudio: Diagnostic_studies País/Región como asunto: Asia Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article