Fengqi Wang

Qingdao University - Medical Genetic Department

Qingdao

China

SCHOLARLY PAPERS

1

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31

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0

Scholarly Papers (1)

1.

Mutations in NKX6.2 Confer Susceptibility to Thyroid Dysgenesis

Number of pages: 47 Posted: 08 Jul 2021
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:

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Thyroid dysgenesis (TD), WES, NKX6.2, Zebrafish, Wnt/β-Catenin signaling pathway