Article Versions Notes

Qi Q, Jiang Y, Zhou X, Meng H, Hao N, Chang J, Bai J, Wang C, Wang M, Guo J, et al. Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes. Genes. 2020; 11(12):1397. https://doi.org/10.3390/genes11121397

Qi, Qingwei, Yulin Jiang, Xiya Zhou, Hua Meng, Na Hao, Jiazhen Chang, Junjie Bai, Chunli Wang, Mingming Wang, Jiangshan Guo, and et al. 2020. "Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes" Genes 11, no. 12: 1397. https://doi.org/10.3390/genes11121397

Qi, Q., Jiang, Y., Zhou, X., Meng, H., Hao, N., Chang, J., Bai, J., Wang, C., Wang, M., Guo, J., Ouyang, Y., Xu, Z., Xiao, M., Zhang, V. W., & Liu, J. (2020). Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes. Genes, 11(12), 1397. https://doi.org/10.3390/genes11121397