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Meiotic chromosome behavior in a human male t(8;15) carrier.
Jiang H, Wang L, Cui Y, Xu Z, Guo T, Cheng D, Xu P, Yu W, Shi Q. Jiang H, et al. J Genet Genomics. 2014 Mar 20;41(3):177-85. doi: 10.1016/j.jgg.2014.01.005. Epub 2014 Jan 28. J Genet Genomics. 2014. PMID: 24656237
MOF influences meiotic expansion of H2AX phosphorylation and spermatogenesis in mice.
Jiang H, Gao Q, Zheng W, Yin S, Wang L, Zhong L, Ali A, Khan T, Hao Q, Fang H, Sun X, Xu P, Pandita TK, Jiang X, Shi Q. Jiang H, et al. Among authors: jiang x. PLoS Genet. 2018 May 24;14(5):e1007300. doi: 10.1371/journal.pgen.1007300. eCollection 2018 May. PLoS Genet. 2018. PMID: 29795555 Free PMC article.
A homozygous FANCM frameshift pathogenic variant causes male infertility.
Yin H, Ma H, Hussain S, Zhang H, Xie X, Jiang L, Jiang X, Iqbal F, Bukhari I, Jiang H, Ali A, Zhong L, Li T, Fan S, Zhang B, Gao J, Li Y, Nazish J, Khan T, Khan M, Zubair M, Hao Q, Fang H, Huang J, Huleihel M, Sha J, Pandita TK, Zhang Y, Shi Q. Yin H, et al. Among authors: jiang x, jiang h, jiang l. Genet Med. 2019 Jan;21(1):62-70. doi: 10.1038/s41436-018-0015-7. Epub 2018 Jun 12. Genet Med. 2019. PMID: 29895858 Free PMC article.
Correction: A homozygous FANCM frameshift pathogenic variant causes male infertility.
Yin H, Ma H, Hussain S, Zhang H, Xie X, Jiang L, Jiang X, Iqbal F, Bukhari I, Jiang H, Ali A, Zhong L, Li T, Fan S, Zhang B, Gao J, Li Y, Nazish J, Khan T, Khan M, Zubair M, Hao Q, Fang H, Huang J, Huleihel M, Sha J, Pandita TK, Zhang Y, Shi Q. Yin H, et al. Among authors: jiang x, jiang h, jiang l. Genet Med. 2019 Jan;21(1):266. doi: 10.1038/s41436-018-0127-0. Genet Med. 2019. PMID: 30158692 Free PMC article.
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