HuGE Literature Finder
Records 1-4
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Novel THRB mutation analysis in congenital hypothyroidism with thyroid dysgenesis.
Journal of cellular biochemistry 2018 Aug . Zhou Zhixia, Yang Chengyu, Lv Fuyan, Liu Wenmiao, Yan Shengli, Zang Hongwei, Li Miaomiao, Wang Fang, Zang Yucui, Liu Shig |
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High frequency of mutations in 'dyshormonogenesis genes' in severe congenital hypothyroidism.
PloS one 2018 13 (9): e0204323. Makretskaya Nina, Bezlepkina Olga, Kolodkina Anna, Kiyaev Alexey, Vasilyev Evgeny V, Petrov Vasily, Kalinenkova Svetlana, Malievsky Oleg, Dedov Ivan I, Tiulpakov Anato |
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Comprehensive screening of eight known causative genes in congenital hypothyroidism with gland-in-situ.
The Journal of clinical endocrinology and metabolism 2016 Aug jc20161879. Nicholas A K, Serra E G, Cangul H, Alyaarubi S, Ullah I, Schoenmakers E, Deeb A, Habeb A M, AlMaghamsi M, Peters C, Nathwani N, Aycan Z, Saglam H, Bober E, Dattani M, Shenoy S, Murray P G, Babiker A, Willemsen R, Thankamony A, Lyons G, Irwin R, Padidela R, Tharian K, Davies J H, Puthi V, Park S-M, Massoud A F, Gregory J W, Albanese A, Pease-Gevers E, Martin H, Brugger K, Maher E R, Chatterjee K, Anderson C A, Schoenmakers |
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Mutation screening of the sodium iodide symporter gene in a cohort of 105 China patients with congenital hypothyroidism.
Arquivos brasileiros de endocrinologia e metabologia 2014 Nov 58 (8): 828-32. Fu Chunyun, Chen Shaoke, Chen Rongyu, Fan Xin, Luo Jingsi, Li Chuan, Qian Jia |
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- Page last updated:Jan 23, 2020
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