Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Congenital Hypothyroidism and GLIS3[original query] |
---|
Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism. Clinica chimica acta; international journal of clinical chemistry 2017 Feb 468 76-80. Fan Xin, Fu Chunyun, Shen Yiping, Li Chuan, Luo Shiyu, Li Qifei, Luo Jingsi, Su Jiasun, Zhang Shujie, Hu Xuyun, Chen Rongyu, Gu Xuefan, Chen Shao |
Mutation screening of the GLIS3 gene in a cohort of 592 Chinese patients with congenital hypothyroidism. Clinica chimica acta; international journal of clinical chemistry 2017 11 476 38-43. Fu Chunyun, Luo Shiyu, Long Xigui, Li Yingfeng, She Shangyang, Hu Xuehua, Mo Meizhen, Wang Zhanghong, Chen Yuhua, He Chun, Su Jiasun, Zhang Yue, Lin Fei, Xie Bobo, Li Qifei, Chen Shao |
Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformations. Clinica chimica acta; international journal of clinical chemistry 2018 12 489 103-108. Fu Chunyun, Luo Shiyu, Zhang Yue, Fan Xin, D'Gama Alissa M, Zhang Xiaofei, Zheng Haiyang, Su Jiasun, Li Chuan, Luo Jingsi, Agrawal Pankaj B, Li Qifei, Chen Shao |
Mutation screening of eight genes and comparison of the clinical data in a Chinese cohort with congenital hypothyroidism. Endocrine 2022 9 79 (1): 125-134. Li Liangshan, Li Xiaole, Wang Xiaoyu, Han Mengmeng, Zhao Dehua, Wang Fang, 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 |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 06, 2024
- Content source: