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Genomic architecture of fetal central nervous system anomalies using whole-genome sequencing.
Yang Y, Zhao S, Sun G, Chen F, Zhang T, Song J, Yang W, Wang L, Zhan N, Yang X, Zhu X, Rao B, Yin Z, Zhou J, Yan H, Huang Y, Ye J, Huang H, Cheng C, Zhu S, Guo J, Xu X, Chen X. Yang Y, et al. Among authors: cheng c. NPJ Genom Med. 2022 May 13;7(1):31. doi: 10.1038/s41525-022-00301-4. NPJ Genom Med. 2022. PMID: 35562572 Free PMC article.
Incidence, distribution, disease spectrum, and genetic deficits of congenital heart defects in China: implementation of prenatal ultrasound screening identified 18,171 affected fetuses from 2,452,249 pregnancies.
Chen X, Zhao S, Dong X, Liu J, Guo Y, Ju W, Chen P, Gao Y, Feng Q, Zhu X, Huang H, Lu X, Yang X, Yang F, Cheng C, Luo X, Cheng L, Zhong N; Chinese Consortium for Prenatal Ultrasound Screening of Congenital Heart Defects. Chen X, et al. Among authors: cheng l, cheng c. Cell Biosci. 2023 Dec 19;13(1):229. doi: 10.1186/s13578-023-01172-7. Cell Biosci. 2023. PMID: 38115160 Free PMC article.
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