Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: SOHLH1[original query] |
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Mutations in SOHLH1 gene associate with nonobstructive azoospermia. Human mutation 2010 Jul 31 (7): 788-93. Choi Youngsok, Jeon Sanghyun, Choi Mikyung, Lee Min-ho, Park Miseon, Lee Dong Ryul, Jun Kyu-Yeon, Kwon Youngjoo, Lee Ok-Hee, Song Seung-Hun, Kim Ji-Young, Lee Kyung-Ah, Yoon Tae Ki, Rajkovic Aleksandar, Shim Sung H |
Association of genetic variants in SOHLH1 and SOHLH2 with non-obstructive azoospermia risk in the Chinese population. European journal of obstetrics, gynecology, and reproductive biology 2015 Jan 184 48-52. Song Bing, Zhang Yan, He Xiao-jin, Du Wei-dong, Ruan Jian, Zhou Fu-sheng, Wu Huan, Zha Xing, Xie Xu-shi, Ye Lei, Wei Zhao-Lian, Zhou Ping, Cao Yun-X |
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency. The Journal of clinical endocrinology and metabolism 2016 Sep jc20162152. Bouilly Justine, Beau Isabelle, Barraud Sara, Bernard Valérie, Azibi Kemal, Fagart Jérôme, Fèvre Anne, Todeschini Anne Laure, Veitia Reiner A, Beldjord Chérif, Delemer Brigitte, Dodé Catherine, Young Jacques, Binart Nadi |
Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations. Andrology 2017 Jul 5 (4): 824-831. Nakamura S, Miyado M, Saito K, Katsumi M, Nakamura A, Kobori Y, Tanaka Y, Ishikawa H, Yoshida A, Okada H, Hata K, Nakabayashi K, Okamura K, Ogata H, Matsubara Y, Ogata T, Nakai H, Fukami |
Next-generation sequencing: toward an increase in the diagnostic yield in patients with apparently idiopathic spermatogenic failure. Asian journal of andrology 2020 Jul . Cannarella Rossella, Condorelli Rosita A, Paolacci Stefano, Barbagallo Federica, Guerri Giulia, Bertelli Matteo, La Vignera Sandro, Calogero Aldo |
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