Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: CLPP[original query] |
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A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family. Journal of clinical research in pediatric endocrinology 2016 Apr . Dursun Fatma, Mohamoud Hussein Sheikh Ali, Karim Noreen, Naeem Muhammad, Jelani Musharraf, K?rm?z?bekmez Hev |
Genetic etiologic analysis in 74 Chinese Han women with idiopathic premature ovarian insufficiency by combined molecular genetic testing. Journal of assisted reproduction and genetics 2021 Feb . Shen Jiandong, Qu Dianyun, Gao Yan, Sun Fangxi, Xie Jiazi, Sun Xueping, Wang Daowu, Ma Xiang, Cui Yugui, Liu Jiayin, Diao Feiya |
Genetic Variants of CLPP and M1AP Are Associated With Risk of Non-Small Cell Lung Cancer. Frontiers in oncology 2021 11 709829. Li Xianghan, Zou Yiran, Li Teng, Wong Thomas K F, Bushey Ryan T, Campa Michael J, Gottlin Elizabeth B, Liu Hongliang, Wei Qingyi, Rodrigo Allen, Patz Edward |
Analysis of copy number variation in men with non-obstructive azoospermia. Andrology 2022 8 10 (8): 1593-1604. Wyrwoll M J, Wabschke R, Röpke A, Wöste M, Ruckert C, Perrey S, Rotte N, Hardy J, Astica L, Lupiáñez D G, Wistuba J, Westernströer B, Schlatt S, Berman A J, Müller A M, Kliesch S, Yatsenko A N, Tüttelmann F, Friedrich |
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