Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Azoospermia and KIT[original query] |
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Mutations in SOHLH1 gene associate with nonobstructive azoospermia. Human mutation 2010 Jul 31 (7): 788-93. Choi Youngsok, Jeon Sanghyun, Choi Mikyung, Lee Min-ho, Park Miseon, Lee Dong Ryul, Jun Kyu-Yeon, Kwon Youngjoo, Lee Ok-Hee, Song Seung-Hun, Kim Ji-Young, Lee Kyung-Ah, Yoon Tae Ki, Rajkovic Aleksandar, Shim Sung H |
PRM1 variant rs35576928 (Arg>Ser) is associated with defective spermatogenesis in the Chinese Han population. Reproductive biomedicine online 2012 Sep . He XJ, Ruan J, Du WD, Chen G, Zhou Y, Xu S, Zuo XB, Cao YX, Zhang XJ |
SNPs in KIT and KITLG genes may be associated with oligospermia in Chinese population. Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2013 Dec 18 (8): 650-4. Cheng Pan, Chen Hui, Liu Shuo-Ran, Pu Xiao-Ying, A Zhou-C |
De novo mutations in idiopathic male infertility-A pilot study. Andrology 2020 8 9 (1): 212-220. Hodži? Alenka, Maver Aleš, Plaseska-Karanfilska Dijana, Ristanovi? Mom?ilo, Noveski Predrag, Zorn Branko, Terzic Marija, Kunej Tanja, Peterlin Bor |
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