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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 4, 2024. (Total: 232145Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Congenital Hypothyroidism and DUOXA1[original query]
DUOX2 and DUOXA2 Variants Confer Susceptibility to Thyroid Dysgenesis and Gland-in-situ With Congenital Hypothyroidism.
Frontiers in endocrinology 2020 5 11 237.
Wang Fengqi, Zang Yucui, Li Miaomiao, Liu Wenmiao, Wang Yangang, Yu Xiaolong, Li Hua, Wang Fang, Liu Shig
Dual Oxidase System Genes Defects in Children With Congenital Hypothyroidism.
Endocrinology 2021 2 162 (8): .
Wang Fengqi, Xiaole Li, Ma Ruixin, Zhao Dehua, Liu Shig
[Genetic mutation profiles for children with congenital hypothyroidism in Fujian province].
Zhonghua yi xue za zhi 2023 2 103 (5): 336-343.
Cheng F, Su Y Q, Wang X R, Wu F Y, Sun F, Fang Y, Zhang R J, Zhao S X, Song H
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