Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: SPEF2[original query] |
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Whole-exome sequencing identified genetic risk factors for asparaginase-related complications in childhood ALL patients. Oncotarget 2017 Jul 8 (27): 43752-43767. Abaji Rachid, Gagné Vincent, Xu Chang Jiang, Spinella Jean-François, Ceppi Francesco, Laverdière Caroline, Leclerc Jean-Marie, Sallan Stephen E, Neuberg Donna, Kutok Jeffery L, Silverman Lewis B, Sinnett Daniel, Krajinovic Ma |
Analysis of a genetic factors contributing to feathering phenotype in chickens. Poultry science 2018 6 97 (10): 3405-3413. Zhang Xiuling, Wang Han, Zhang Lechao, Wang Qi, Du Xiaolong, Ge Linhan, Zhou Rongyan, Li Lanhui, Li Xianglo |
Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility. Journal of medical genetics 2019 5 57 (1): 31-37. Liu Chunyu, Lv Mingrong, He Xiaojin, Zhu Yong, Amiri-Yekta Amir, Li Weiyu, Wu Huan, Kherraf Zine-Eddine, Liu Wangjie, Zhang Jingjing, Tan Qing, Tang Shuyan, Zhu Yong-Jun, Zhong Yading, Li Caihua, Tian Shixiong, Zhang Zhiguo, Jin Li, Ray Pierre, Zhang Feng, Cao Yunx |
Family-based exome sequencing identifies rare coding variants in age-related macular degeneration. Human molecular genetics 2020 Apr . Ratnapriya Rinki, Acar ?lhan E, Geerlings Maartje J, Branham Kari, Kwong Alan, Saksens Nicole T M, Pauper Marc, Corominas Jordi, Kwicklis Madeline, Zipprer David, Starostik Margaret R, Othman Mohammad, Yashar Beverly, Abecasis Goncalo R, Chew Emily Y, Ferrington Deborah A, Hoyng Carel B, Swaroop Anand, den Hollander Anneke |
Novel HYDIN variants associated with male infertility in two Chinese families. Frontiers in endocrinology 2023 2 14 1118841. Yu Hui, Shi Xiao, Shao Zhongmei, Geng Hao, Guo Senzhao, Li Kuokuo, Gu Meng, Xu Chuan, Gao Yang, Tan Qing, Duan Zongliu, Wu Huan, Hua Rong, Guo Rui, Wei Zhaolian, Zhou Ping, Cao Yunxia, He Xiaojin, Li Liang, Zhang Xiaoping, Lv Mingro |
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