Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Azoospermia and PRDM9[original query] |
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Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest. Journal of assisted reproduction and genetics 0 25 (11-12): 553-7. Miyamoto Toshinobu, Koh Eitetsu, Sakugawa Naoko, Sato Hisashi, Hayashi Hiroaki, Namiki Mikio, Sengoku Kaz |
Single-nucleotide polymorphisms of the PRDM9 (MEISETZ) gene in patients with nonobstructive azoospermia. Journal of andrology 0 30 (4): 426-31. Irie Shinji, Tsujimura Akira, Miyagawa Yasushi, Ueda Tomohiro, Matsuoka Yasuhiro, Matsui Yasuhisa, Okuyama Akihiko, Nishimune Yoshitake, Tanaka Hiromit |
PRDM9 gene polymorphism may not be associated with defective spermatogenesis in the Chinese Han population. Systems biology in reproductive medicine 2013 Feb 59 (1): 38-41. He Xiao-Jin, Ruan Jian, Du Wei-Dong, Cao Yun-Xia, Chen Gang, Zuo Xian-Bo, Peng Yu-Wan, Wu Huan, Song Bing, Zhang Xue-J |
Association of Single Nucleotide Polymorphisms in the PYGO2 and PRDM9 Genes with Idiopathic Azoospermia in Iranian Infertile Male Patients. Iranian journal of medical sciences 2023 1 48 (1): 77-84. Soleymani Moud Sanaz, Kamal Seraji Katayun, Ramezani Mina, Piravar Zeyn |
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- Page last updated:Jun 11, 2024
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