Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Hypothyroidism and PROP1[original query] |
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Mutation spectrum analysis of 29 causative genes in 43 Chinese patients with congenital hypothyroidism. Molecular medicine reports 2020 Apr . Wang Huijuan, Kong Xiaohong, Pei Yanrui, Cui Xuemei, Zhu Yijie, He Zixuan, Wang Yanxia, Zhang Lirong, Zhuo Lixia, Chen Chao, Yan Xiao |
Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency. Journal of clinical research in pediatric endocrinology 2020 1 12 (3): 261-268. Bulut Fatma Derya, Özdemir Dilek Semine, Kotan Damla, Mengen Eda, Gürbüz Fatih, Yüksel Bilg |
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- Page last updated:Mar 25, 2024
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