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Identification of loss-of-function HOXA2 mutations in Chinese families with dominant bilateral microtia.
Si, Nuo; Meng, Xiaolu; Lu, Xiaosheng; Zhao, Xuelian; Li, Chuan; Yang, Meirong; Zhang, Ye; Wang, Changchen; Guo, Peipei; Zhang, Xue; Pan, Bo; Jiang, Haiyue.
Affiliation
  • Si N; Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, China; Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, School of Basic Medicine Peking Union Medical College, China.
  • Meng X; Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, School of Basic Medicine Peking Union Medical College, China.
  • Lu X; Department of Plastic Surgery, Affiliated Hospital of Weifang Medical University, China.
  • Zhao X; Department of Plastic Surgery, The Second Hospital of Hebei Medical University, China.
  • Li C; Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, China.
  • Yang M; Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, China.
  • Zhang Y; Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, China.
  • Wang C; Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, China.
  • Guo P; Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, China.
  • Zhang X; Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, School of Basic Medicine Peking Union Medical College, China.
  • Pan B; Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, China. Electronic address: 13810855912@163.com.
  • Jiang H; Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, China. Electronic address: haiyuejiang2019@163.com.
Gene ; 757: 144945, 2020 Oct 05.
Article de En | MEDLINE | ID: mdl-32649979
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Protéines à homéodomaine / Microtie congénitale / Mutation perte de fonction Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Female / Humans / Male Langue: En Journal: Gene Année: 2020 Type de document: Article Pays d'affiliation: Chine Pays de publication: Pays-Bas
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Protéines à homéodomaine / Microtie congénitale / Mutation perte de fonction Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Female / Humans / Male Langue: En Journal: Gene Année: 2020 Type de document: Article Pays d'affiliation: Chine Pays de publication: Pays-Bas