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Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism

Authors

  • Chunyun Fu Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  • Bobo Xie Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  • Shujie Zhang Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  • Jin Wang Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  • Shiyu Luo Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  • Haiyang Zheng Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  • Jiasun Su Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  • Xuyun Hu Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  • Rongyu Chen Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  • Xin Fan Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  • Jingsi Luo Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  • Xuefan Gu Endocrinology and Genetic Metabolism of Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China PubMed articlesGoogle scholar articles
  • Shaoke Chen Department of Genetic Metabolism, Children's Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China Guangxi Center for Birth Defects Research and Prevention, Nanning, People's Republic of China PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Shaoke Chen; chenshaoke123{at}163.com
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Citation

Fu C, Xie B, Zhang S, et al
Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism

Publication history

  • Received December 1, 2015
  • Revised March 26, 2016
  • Accepted April 5, 2016
  • First published May 12, 2016.
Online issue publication 
October 25, 2017

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