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Novel STAMBP mutations in a Chinese girl with rare symptoms of microcephaly-capillary malformation syndrome and Mowat-Wilson syndrome.
Wang, Hui; Wang, Zhan; Ji, Taoyun; Tai, Jun; Jiang, Qian.
Afiliación
  • Wang H; Department of Pediatrics, Tongzhou Maternal and Child Health Hospital of Beijing, Beijing 101100, China.
  • Wang Z; Department of Medical Genetics, Capital Institute of Pediatrics, Beijing 100020, China.
  • Ji T; Department of Otolaryngology Head and Neck Surgery, Children's Hospital, Capital Institute of Pediatrics, Beijing 100020, China.
  • Tai J; Department of Pediatrics, Peking University First Hospital, Beijing, 100034, China.
  • Jiang Q; Department of Otolaryngology Head and Neck Surgery, Children's Hospital, Capital Institute of Pediatrics, Beijing 100020, China.
Heliyon ; 9(12): e22989, 2023 Dec.
Article en En | MEDLINE | ID: mdl-38058451
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Heliyon Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Heliyon Año: 2023 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido