Your browser doesn't support javascript.
loading
[Genotype and phenotype analysis of a family with Waardenburg syndrome type Ⅰcaused by a novel mutation in PAX3 gene].
Li, Xia; Zhao, Shengbo; Bi, Xianyun; Lou, Fan; Zeng, Wenjuan; Gao, Yan; Mao, Zhiyong; Ma, Jing.
Afiliação
  • Li X; Department of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
  • Zhao S; Department of Otolaryngology Head and Neck Surgery，Zhaotong First People's Hospital.
  • Bi X; Department of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
  • Lou F; Department of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
  • Zeng W; Department of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
  • Gao Y; Department of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
  • Mao Z; Department of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
  • Ma J; Department of Otolaryngology Head and Neck Surgery，Kunming Children's Hospital，（Children's Hospital Affiliated to Kunming Medical University），Kunming，650228，China.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi ; 35(7): 621-626, 2021 Jul.
Article em Zh | MEDLINE | ID: mdl-34304492
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Síndrome de Waardenburg Tipo de estudo: Prognostic_studies Limite: Humans País/Região como assunto: Asia Idioma: Zh Revista: Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Síndrome de Waardenburg Tipo de estudo: Prognostic_studies Limite: Humans País/Região como assunto: Asia Idioma: Zh Revista: Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi Ano de publicação: 2021 Tipo de documento: Article