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Weibing Tian
Weifang Medical University
Weifang
China
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SCHOLARLY PAPERS
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Scholarly Papers (1)
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1.
Mutations in
NKX6.2
Confer Susceptibility to Thyroid Dysgenesis
Number of pages: 47
Posted: 08 Jul 2021
Jingjing Niu
,
Liangshan Li
,
Yangang Wang
,
Liqin Zhang
,
Fang Wang
,
Dehua Zhao
,
Maosheng Gu
,
Hui Zou
,
Wei Li
,
Longfang Xu
,
Fengqi Wang
,
Miaomiao Li
,
Yucui Zang
, Weibing Tian,
Yulin Zhou
,
Wenbin Zhu
,
Quanqi Zhang
and
Shiguo Liu
Ocean University of China, Qingdao University - Medical Genetic Department, Qingdao University - Department of Endocrinology and Metabolism, Qingdao Women & Children Hospital - Neonatal Screening Center, Qingdao University - Department of Endocrinology and Metabolism, Zhengzhou University - Department of Henan Newborn Screening Center, Xuzhou Medical University - Newborn Screening Center, Jinan Maternity and Child Health Care Hospital - Neonatal Disease Screening Center, Hebei Medical University - Neonatal Disease Screening Center, Heze Maternal and Child Health-Care Hospital - Department of Neonatal Screening Center, Qingdao University - Medical Genetic Department, Qingdao University - Medical Genetic Department, Qingdao University - Medical Genetic Department, Weifang Medical University, Xiamen University - School of Public Health, Fujian Maternal and Children Health Hospital - Fujian Neonatal Screening Center, Ocean University of China - MOE Key Laboratory of Marine Genetics and Breeding and Qingdao University - Medical Genetic Department
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Abstract:
Thyroid dysgenesis (TD), WES, NKX6.2, Zebrafish, Wnt/β-Catenin signaling pathway
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