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Acknowledgements
We thank Xiaojun Ren, Baozhu Cai, Qing Chen, Yanhua Wu, Hexige Saiyin, Xuan Zhang, Shuangjie Wang, Xi Yang and Wangjie Liu for their help in experiments and constructive suggestions. We also thank the Genome Tagging Project Center for technical support. This work was supported by National Natural Science Foundation of China (31625015, 31521003, 81571404 and 31771396), Shanghai Municipal Commission for Science and Technology (18ZR1432300, 19QA1407500 and 17JC1400900), China Postdoctoral Science Foundation (2018T110340 and 2017M621349), Shanghai Hospital Development Center (SHDC12015117), Shanghai Medical Center of Key Programs for Female Reproductive Diseases (2017ZZ01016), and Shanghai Municipal Science and Technology Major Project (2017SHZDZX01).
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L.W., S.D. and F.Z. designed the experiments, interpreted the data and wrote the manuscript, with help from all authors. Y.Z., N.Z. and K.H. provided the clinical data. L.W., X.F., S.D., C.S., N.Y. and L.Z. performed the experiments. L.W., Y.Z., X.F., S.D., S.T., N.Z., H.W., H.S., L.J., F.Z., J.L. and K.H. analyzed the data. F.Z., K.H., J.L., L.W. and S.D. supervised the experiments. All authors discussed the results and commented on the manuscript.
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Wang, L., Zhang, Y., Fu, X. et al. Joint utilization of genetic analysis and semi-cloning technology reveals a digenic etiology of Müllerian anomalies. Cell Res 30, 91–94 (2020). https://doi.org/10.1038/s41422-019-0243-7
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DOI: https://doi.org/10.1038/s41422-019-0243-7
