Your browser doesn't support javascript.
loading
Nf1 in heart development: a potential causative gene for congenital heart disease: a narrative review.
Wang, Dun; Wen, Xue; Xu, Li-Li; Chen, Qing-Xing; Yan, Tian-Xing; Xiao, Hai-Tao; Xu, Xue-Wen.
Afiliación
  • Wang D; Department of Burn and Plastic Surgery, West China Hospital of Sichuan University, Chengdu, People's Republic of China.
  • Wen X; Department of Burn and Plastic Surgery, West China Hospital of Sichuan University, Chengdu, People's Republic of China.
  • Xu LL; Department of Cardiology, Zhongshan Hospital, Fudan University, Shanghai Institute of Cardiovascular Diseases, Shanghai, People's Republic of China.
  • Chen QX; Department of Cardiology, Zhongshan Hospital, Fudan University, Shanghai Institute of Cardiovascular Diseases, Shanghai, People's Republic of China.
  • Yan TX; Central Laboratory, National Clinical Research Center for Oral Diseases, Peking University School and Hospital of Stomatology, Beijing, People's Republic of China.
  • Xiao HT; Department of Burn and Plastic Surgery, West China Hospital of Sichuan University, Chengdu, People's Republic of China.
  • Xu XW; Department of Burn and Plastic Surgery, West China Hospital of Sichuan University, Chengdu, People's Republic of China.
Physiol Genomics ; 55(10): 415-426, 2023 10 01.
Article en En | MEDLINE | ID: mdl-37519249
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Neurofibromatosis 1 / Cardiopatías Congénitas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Physiol Genomics Asunto de la revista: BIOLOGIA MOLECULAR Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Neurofibromatosis 1 / Cardiopatías Congénitas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Physiol Genomics Asunto de la revista: BIOLOGIA MOLECULAR Año: 2023 Tipo del documento: Article