Wang Fengqi

3PUBLICATIONS
3CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsDevelopmental genetics (incl. sex determination)
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Publications (3)

|Feb 24, 2025
Common and Rare DUOX Variants in Patients With Congenital Hypothyroidism: Case-control Study and Family-based Analysis.

Yaning Jia, Xiaoyu Wang, Liqin Zhang

|Oct 30, 2024
Analysis of the genetic etiology of CDH23 gene variation in a child with hearing loss.

Zhong Xue, Wang Yingzi, Jia Yaning

|Feb 25, 2021
Dual Oxidase System Genes Defects in Children With Congenital Hypothyroidism.

Fengqi Wang, Li Xiaole, Ruixin Ma

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