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Identifying occult maternal malignancies from 1.93 million pregnant women undergoing noninvasive prenatal screening tests.
Ji X, Li J, Huang Y, Sung PL, Yuan Y, Liu Q, Chen Y, Ju J, Zhou Y, Huang S, Chen F, Han Y, Yuan W, Fan C, Zhao Q, Wu H, Feng S, Liu W, Li Z, Chen J, Chen M, Yao H, Zeng L, Ma T, Fan S, Zhang J, Yuen KY, Cheng SH, Chik IWS, Liu NT, Zhu J, Lin S, Cao J, Tong S, Shan Z, Li W, Hekmat MR, Garshasbi M, Suela J, Torres Y, Cigudosa JC, Ruiz FJP, Rodríguez L, García M, Bernik J, Traven E, Reš U, Tul N, Tseng CF, Zhao D, Sun L, Pan Q, Shen L, Dai M, Wang Y, Wang J, Yang H, Yin Y, Duan T, Zhu B, Choolani M, Jin X, Chen Y, Mao M. Ji X, et al. Among authors: duan t. Genet Med. 2019 Oct;21(10):2293-2302. doi: 10.1038/s41436-019-0510-5. Epub 2019 Apr 12. Genet Med. 2019. PMID: 30976098 Free article.
The physiologic pattern of normal labour progression.
Zhang J, Duan T. Zhang J, et al. Among authors: duan t. BJOG. 2018 Jul;125(8):955. doi: 10.1111/1471-0528.14929. Epub 2017 Nov 3. BJOG. 2018. PMID: 28889657 No abstract available.
Screening for preeclampsia in low-risk twin pregnancies at early gestation.
Chen J, Zhao D, Liu Y, Zhou J, Zou G, Zhang Y, Guo M, Duan T, Van Mieghem T, Sun L. Chen J, et al. Among authors: duan t. Acta Obstet Gynecol Scand. 2020 Oct;99(10):1346-1353. doi: 10.1111/aogs.13890. Epub 2020 May 17. Acta Obstet Gynecol Scand. 2020. PMID: 32356359 Free article.
Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors.
Dan S, Wang W, Ren J, Li Y, Hu H, Xu Z, Lau TK, Xie J, Zhao W, Huang H, Xie J, Sun L, Zhang X, Wang W, Liao S, Qiang R, Cao J, Zhang Q, Zhou Y, Zhu H, Zhong M, Guo Y, Lin L, Gao Z, Yao H, Zhang H, Zhao L, Jiang F, Chen F, Jiang H, Li S, Li Y, Wang J, Wang J, Duan T, Su Y, Zhang X. Dan S, et al. Among authors: duan t. Prenat Diagn. 2012 Dec;32(13):1225-32. doi: 10.1002/pd.4002. Epub 2012 Nov 9. Prenat Diagn. 2012. PMID: 23138752 Clinical Trial.
Whole Genome Sequencing in the Evaluation of Fetal Structural Anomalies: A Parallel Test with Chromosomal Microarray Plus Whole Exome Sequencing.
Zhou J, Yang Z, Sun J, Liu L, Zhou X, Liu F, Xing Y, Cui S, Xiong S, Liu X, Yang Y, Wei X, Zou G, Wang Z, Wei X, Wang Y, Zhang Y, Yan S, Wu F, Zeng F, Wang J, Duan T, Peng Z, Sun L. Zhou J, et al. Among authors: duan t. Genes (Basel). 2021 Mar 6;12(3):376. doi: 10.3390/genes12030376. Genes (Basel). 2021. PMID: 33800913 Free PMC article.
789 results