檢索結果 - Shi‐Min Yuan
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Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans 由 Yue‐Qiu Tan, Chaofeng Tu, Lanlan Meng, Shi‐Min Yuan, Calvin Sjaarda, Aixiang Luo, Juan Du, Wen Li, Fei Gong, Changgao Zhong, Han‐Xiang Deng, Guangxiu Lu, Ping Liang, Ge Lin
出版 2017Artigo -
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Biallelic mutations in <i>CFAP65</i> lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations 由 Weili Wang, Chaofeng Tu, Hongchuan Nie, Lanlan Meng, Yong Li, Shi‐Min Yuan, Victor Wei Zhang, Juan Du, Junpu Wang, Fei Gong, Li-Qing Fan, Guangxiu Lu, Ge Lin, Yue‐Qiu Tan
出版 2019Artigo
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