Your browser doesn't support javascript.
loading
[Genetic mutation profiles for children with congenital hypothyroidism in Fujian province].
Cheng, F; Su, Y Q; Wang, X R; Wu, F Y; Sun, F; Fang, Y; Zhang, R J; Zhao, S X; Song, H D.
Afiliação
  • Cheng F; College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Department of Clinical Laboratory, Fujian Children's Hospital, Fuzhou 350001, China.
  • Su YQ; College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Department of Clinical Laboratory, Fujian Maternity and Child Health Hospital, Fuzhou 350001, China.
  • Wang XR; College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Medical Reaseach Center, Fujian Maternity and Child Health Hospital, Fuzhou 350001, China.
  • Wu FY; Department of Molecular Diagnostics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai 200011, China.
  • Sun F; Department of Molecular Diagnostics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai 200011, China.
  • Fang Y; Department of Molecular Diagnostics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai 200011, China.
  • Zhang RJ; Department of Molecular Diagnostics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai 200011, China.
  • Zhao SX; Department of Molecular Diagnostics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai 200011, China.
  • Song HD; Department of Molecular Diagnostics, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai 200011, China.
Zhonghua Yi Xue Za Zhi ; 103(5): 336-343, 2023 Feb 07.
Article em Zh | MEDLINE | ID: mdl-36740391
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipotireoidismo Congênito Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Female / Humans / Male / Newborn Idioma: Zh Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipotireoidismo Congênito Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Female / Humans / Male / Newborn Idioma: Zh Ano de publicação: 2023 Tipo de documento: Article