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Mutation analysis of FBN1 gene in two Chinese families with congenital ectopia lentis in northern China.
Tang, Su-Zhen; Liu, Ya-Ning; Hu, Shao-Hua; Chen, Hao; Zhao, Hui; Feng, Xue-Mei; Pan, Xiao-Jing; Chen, Peng.
Afiliação
  • Tang SZ; Department of Human Anatomy, Histology and Embryology, School of Basic Medicine, Qingdao University, Qingdao 266071, Shandong Province, China.
  • Liu YN; Department of Human Anatomy, Histology and Embryology, School of Basic Medicine, Qingdao University, Qingdao 266071, Shandong Province, China.
  • Hu SH; Department of Human Anatomy, Histology and Embryology, School of Basic Medicine, Qingdao University, Qingdao 266071, Shandong Province, China.
  • Chen H; Department of Human Anatomy, Histology and Embryology, School of Basic Medicine, Qingdao University, Qingdao 266071, Shandong Province, China.
  • Zhao H; The 971 Hospital of the Chinese People's Liberation Army Navy, Qingdao 266071, Shandong Province, China.
  • Feng XM; Department of Human Anatomy, Histology and Embryology, School of Basic Medicine, Qingdao University, Qingdao 266071, Shandong Province, China.
  • Pan XJ; Qingdao Eye Hospital, Shandong Eye Institute, Shandong First Medical University & Shandong Academy of Medical Sciences, Qingdao 266071, Shandong Province, China.
  • Chen P; Department of Human Anatomy, Histology and Embryology, School of Basic Medicine, Qingdao University, Qingdao 266071, Shandong Province, China.
Int J Ophthalmol ; 12(11): 1674-1679, 2019.
Article em En | MEDLINE | ID: mdl-31741853
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Int J Ophthalmol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Int J Ophthalmol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China