Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Hypogonadism and DCC[original query] |
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DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development. Human molecular genetics 2017 12 27 (2): 359-372. Bouilly Justine, Messina Andrea, Papadakis Georgios, Cassatella Daniele, Xu Cheng, Acierno James S, Tata Brooke, Sykiotis Gerasimos, Santini Sara, Sidis Yisrael, Elowe-Gruau Eglantine, Phan-Hug Franziska, Hauschild Michael, Bouloux Pierre-Marc, Quinton Richard, Lang-Muritano Mariarosaria, Favre Lucie, Marino Laura, Giacobini Paolo, Dwyer Andrew A, Niederländer Nicolas J, Pitteloud Nel |
Whole exome sequencing and trio analysis to broaden the variant spectrum of genes in idiopathic hypogonadotropic hypogonadism. Asian journal of andrology 2020 11 23 (3): 288-293. Zhang Jian, Tang Shu-Yan, Zhu Xiao-Bin, Li Peng, Lu Jian-Qi, Cong Jiang-Shan, Wang Ling-Bo, Zhang Feng, Li Zhe |
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- Page last updated:Apr 29, 2024
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