Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: KLHL10[original query] |
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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 |
Development of a novel next-generation sequencing panel for diagnosis of quantitative spermatogenic impairment. Journal of assisted reproduction and genetics 2020 4 37 (4): 753-762. Rocca Maria Santa, Msaki Aichi, Ghezzi Marco, Cosci Ilaria, Pilichou Kalliopi, Celeghin Rudy, Foresta Carlo, Ferlin Alber |
The I510V mutation in KLHL10 in a patient with oligoasthenoteratozoospermia. The Journal of reproduction and development 2021 8 67 (5): 313-318. Huang Zicong, Chen Feilong, Xie Minyu, Zhang Hanbin, Zhuang Yuge, Huang Chuyu, Li Xuemei, Liu Hong, Chen Zheng |
Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot. Translational pediatrics 2023 11 12 (10): 1835-1841. Yu Pan, Manli Liu, Songsong Zhang, Huaxian Mei, Jing |
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- Page last updated:Apr 22, 2024
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