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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 4, 2023. (Total: 223640Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Azoospermia and KIT[original query]
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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