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Homozygous Mutations in BTG4 Cause Zygotic Cleavage Failure and Female Infertility.
Zheng W, Zhou Z, Sha Q, Niu X, Sun X, Shi J, Zhao L, Zhang S, Dai J, Cai S, Meng F, Hu L, Gong F, Li X, Fu J, Shi R, Lu G, Chen B, Fan H, Wang L, Lin G, Sang Q. Zheng W, et al. Among authors: wang l. Am J Hum Genet. 2020 Jul 2;107(1):24-33. doi: 10.1016/j.ajhg.2020.05.010. Epub 2020 Jun 4. Am J Hum Genet. 2020. PMID: 32502391 Free PMC article.
Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest.
Xu Y, Shi Y, Fu J, Yu M, Feng R, Sang Q, Liang B, Chen B, Qu R, Li B, Yan Z, Mao X, Kuang Y, Jin L, He L, Sun X, Wang L. Xu Y, et al. Among authors: wang l. Am J Hum Genet. 2016 Sep 1;99(3):744-752. doi: 10.1016/j.ajhg.2016.06.024. Epub 2016 Aug 18. Am J Hum Genet. 2016. PMID: 27545678 Free PMC article.
Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility.
Sang Q, Li B, Kuang Y, Wang X, Zhang Z, Chen B, Wu L, Lyu Q, Fu Y, Yan Z, Mao X, Xu Y, Mu J, Li Q, Jin L, He L, Wang L. Sang Q, et al. Among authors: wang x, wang l. Am J Hum Genet. 2018 Apr 5;102(4):649-657. doi: 10.1016/j.ajhg.2018.02.015. Epub 2018 Mar 29. Am J Hum Genet. 2018. PMID: 29606300 Free PMC article.
The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility.
Chen B, Wang W, Peng X, Jiang H, Zhang S, Li D, Li B, Fu J, Kuang Y, Sun X, Wang X, Zhang Z, Wu L, Zhou Z, Lyu Q, Yan Z, Mao X, Xu Y, Mu J, Li Q, Jin L, He L, Sang Q, Wang L. Chen B, et al. Among authors: wang x, wang w, wang l. Eur J Hum Genet. 2019 Feb;27(2):300-307. doi: 10.1038/s41431-018-0283-3. Epub 2018 Oct 8. Eur J Hum Genet. 2019. PMID: 30297906 Free PMC article.
Bi-allelic Missense Pathogenic Variants in TRIP13 Cause Female Infertility Characterized by Oocyte Maturation Arrest.
Zhang Z, Li B, Fu J, Li R, Diao F, Li C, Chen B, Du J, Zhou Z, Mu J, Yan Z, Wu L, Liu S, Wang W, Zhao L, Dong J, He L, Liang X, Kuang Y, Sun X, Sang Q, Wang L. Zhang Z, et al. Among authors: wang w, wang l. Am J Hum Genet. 2020 Jul 2;107(1):15-23. doi: 10.1016/j.ajhg.2020.05.001. Epub 2020 May 29. Am J Hum Genet. 2020. PMID: 32473092 Free PMC article.
Novel mutations in LHCGR (luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome.
Zhang Z, Wu L, Diao F, Chen B, Fu J, Mao X, Yan Z, Li B, Mu J, Zhou Z, Wang W, Zhao L, Dong J, Zeng Y, Du J, Kuang Y, Sun X, He L, Sang Q, Wang L. Zhang Z, et al. Among authors: wang w, wang l. J Assist Reprod Genet. 2020 Nov;37(11):2861-2868. doi: 10.1007/s10815-020-01931-2. Epub 2020 Aug 28. J Assist Reprod Genet. 2020. PMID: 32860205 Free PMC article.
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