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For: Wang F, Guo S, Li P. Two novel mutations in the MCM8 gene shared by two Chinese siblings with primary ovarian insufficiency and short stature. Mol Genet Genomic Med 2020;8:e1396. [PMID: 32652893 DOI: 10.1002/mgg3.1396] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Huang C, Guo T, Qin Y. Meiotic Recombination Defects and Premature Ovarian Insufficiency. Front Cell Dev Biol 2021;9:652407. [PMID: 33763429 DOI: 10.3389/fcell.2021.652407] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
2 Wang F, Guo S, Li P. Two novel mutations in the MCM8 gene shared by two Chinese siblings with primary ovarian insufficiency and short stature. Mol Genet Genomic Med 2020;8:e1396. [PMID: 32652893 DOI: 10.1002/mgg3.1396] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
3 Li J, Yu D, Liu L, Liang H, Ouyang Q, Liu Y. Structural study of the N-terminal domain of human MCM8/9 complex. Structure 2021:S0969-2126(21)00164-7. [PMID: 34043945 DOI: 10.1016/j.str.2021.05.006] [Reference Citation Analysis]
4 Cioppi F, Rosta V, Krausz C. Genetics of Azoospermia. Int J Mol Sci 2021;22:3264. [PMID: 33806855 DOI: 10.3390/ijms22063264] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]