Chen M - Search Results

1

Noninvasive prenatal diagnosis for Duchenne muscular dystrophy based on the direct haplotype phasing.

Chen M, Chen C, Huang X, Sun J, Jiang L, Li Y, Zhu Y, Tian C, Li Y, Lu Z, Wang Y, Zeng F, Yang Y, Song X, Peng Z, Yin C, Chen D. Chen M, et al. Among authors: chen c, chen d. Prenat Diagn. 2020 Jul;40(8):918-924. doi: 10.1002/pd.5641. Epub 2020 Jun 4. Prenat Diagn. 2020. PMID: 31916613

2

Noninvasive prenatal testing of trisomies 21 and 18 by massively parallel sequencing of maternal plasma DNA in twin pregnancies.

Huang X, Zheng J, Chen M, Zhao Y, Zhang C, Liu L, Xie W, Shi S, Wei Y, Lei D, Xu C, Wu Q, Guo X, Shi X, Zhou Y, Liu Q, Gao Y, Jiang F, Zhang H, Su F, Ge H, Li X, Pan X, Chen S, Chen F, Fang Q, Jiang H, Lau TK, Wang W. Huang X, et al. Among authors: chen m, chen s, chen f. Prenat Diagn. 2014 Apr;34(4):335-40. doi: 10.1002/pd.4303. Epub 2014 Feb 3. Prenat Diagn. 2014. PMID: 24357023

3

Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome.

Chen M, Chan JK, Nadarajah S, Tan AS, Chan ML, Mathew J, Saw EE, Lim C, Wong W, Cheah FS, Law HY, Wong PC, Chong SS. Chen M, et al. Prenat Diagn. 2015 Jun;35(6):534-43. doi: 10.1002/pd.4568. Epub 2015 Mar 1. Prenat Diagn. 2015. PMID: 25641621

4

Identify Down syndrome transcriptome associations using integrative analysis of microarray database and correlation-interaction network.

Chen M, Wang J, Luo Y, Huang K, Shi X, Liu Y, Li J, Lai Z, Xue S, Gao H, Chen A, Chen D. Chen M, et al. Among authors: chen a, chen d. Hum Genomics. 2018 Jan 19;12(1):2. doi: 10.1186/s40246-018-0133-y. Hum Genomics. 2018. PMID: 29351810 Free PMC article.

5

Prenatal diagnose of a fetus with Harlequin ichthyosis in a Chinese family.

Jian W, Du QT, Lai ZF, Li YF, Li SQ, Xiong ZT, Chen DJ, Chen M, Chen JS. Jian W, et al. Among authors: chen m, chen js, chen dj. Taiwan J Obstet Gynecol. 2018 Jun;57(3):452-455. doi: 10.1016/j.tjog.2018.04.023. Taiwan J Obstet Gynecol. 2018. PMID: 29880184 Free article.

6

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: chen j, chen m, chen f, chen y. 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.

7

Haplotype-Based noninvasive prenatal diagnosis for duchenne muscular dystrophy: A pilot study in South China.

Chen M, Chen C, Li Y, Yuan Y, Lai Z, Guo F, Wang Y, Huang X, Li S, Wu R, Peng Z, Sun J, Chen D. Chen M, et al. Among authors: chen c, chen d. Eur J Obstet Gynecol Reprod Biol. 2019 Sep;240:15-22. doi: 10.1016/j.ejogrb.2019.05.005. Epub 2019 May 8. Eur J Obstet Gynecol Reprod Biol. 2019. PMID: 31207536

8

Noninvasive prenatal diagnosis of β-thalassemia by relative haplotype dosage without analyzing proband.

Li H, Du B, Jiang F, Guo Y, Wang Y, Zhang C, Zeng X, Xie Y, Ouyang S, Xian Y, Chen M, Liu W, Sun X. Li H, et al. Among authors: chen m. Mol Genet Genomic Med. 2019 Nov;7(11):e963. doi: 10.1002/mgg3.963. Epub 2019 Sep 30. Mol Genet Genomic Med. 2019. PMID: 31566929 Free PMC article.

9

Validation of fetal DNA fraction estimation and its application in noninvasive prenatal testing for aneuploidy detection in multiple pregnancies.

Chen M, Jiang F, Guo Y, Yan H, Wang J, Zhang L, Zeng X, Li S, Li Y, Li N, Zhang C, Zhu W, Du B, Wang Y, Lan Z, Luo X, Luo F, Chen D. Chen M, et al. Among authors: chen d. Prenat Diagn. 2019 Dec;39(13):1273-1282. doi: 10.1002/pd.5597. Epub 2019 Nov 11. Prenat Diagn. 2019. PMID: 31671222

10

L1CAM mutations in three fetuses diagnosed by medical exome sequencing.

Li YT, Chen JS, Jian W, He YD, Li N, Xie YN, Wang J, Zhang VW, Huang WR, Jiang FM, Ye XQ, Chen DJ, Chen M. Li YT, et al. Among authors: chen m, chen js, chen dj. Taiwan J Obstet Gynecol. 2020 May;59(3):451-455. doi: 10.1016/j.tjog.2020.03.022. Taiwan J Obstet Gynecol. 2020. PMID: 32416898 Free article.

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