Dong M - Search Results

1

Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples.

Qian Y, Sun Y, Guo X, Song L, Sun Y, Gao X, Liu B, Xu Y, Chen N, Chen M, Luo Y, Qiao Z, Fan L, Man J, Zhang K, Wang X, Rong T, Wang Z, Liu F, Zhao J, Wei X, Chen M, Peng Z, Peng H, Sun J, Dong M. Qian Y, et al. Among authors: dong m. J Med Genet. 2023 Oct;60(10):933-938. doi: 10.1136/jmg-2022-109112. Epub 2023 Apr 3. J Med Genet. 2023. PMID: 37012053

2

Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease.

Liu B, Chen SC, Yang YM, Yan K, Qian YQ, Zhang JY, Hu YT, Dong MY, Jin F, Huang HF, Xu CM. Liu B, et al. Sci Rep. 2015 Dec 3;5:17468. doi: 10.1038/srep17468. Sci Rep. 2015. PMID: 26632257 Free PMC article.

3

Detection of fetal duplication 16p11.2q12.1 by next-generation sequencing of maternal plasma and invasive diagnosis.

Chen M, Fu XY, Luo YQ, Qian YQ, Pan L, Wang LY, Dong MY. Chen M, et al. Among authors: dong my. J Matern Fetal Neonatal Med. 2019 Jan;32(1):38-45. doi: 10.1080/14767058.2017.1369947. Epub 2017 Sep 7. J Matern Fetal Neonatal Med. 2019. PMID: 28882078

4

[Detection of cell-free fetal DNA in maternal plasma for noninvasive prenatal screening of fetal chromosomal aneuploidies in women of advanced maternal age].

Zhu H, Miao Z, Qian Y, Li H, Jin J, He J, Dong M. Zhu H, et al. Among authors: dong m. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017 May 25;46(3):256-261. doi: 10.3785/j.issn.1008-9292.2017.06.05. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017. PMID: 29039166 Free PMC article. Chinese.

5

[Single nucleotide polymorphism-array in genetic analysis of chorionic villi from early spontaneous miscarriages].

Sun Y, Luo Y, Qian Y, Dong M, Jin F. Sun Y, et al. Among authors: dong m. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017 May 25;46(3):262-267. doi: 10.3785/j.issn.1008-9292.2017.06.06. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017. PMID: 29039167 Free PMC article. Chinese.

6

[Advances in the application of high-throughput sequencing in clinical genetics].

Qian Y, Wang L, Luo Y, Yan K, Dong M, Jin F. Qian Y, et al. Among authors: dong m. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017 May 25;46(3):334-337. doi: 10.3785/j.issn.1008-9292.2017.06.18. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017. PMID: 29039179 Free PMC article. Chinese. No abstract available.

7

A feasible diagnostic approach for the translocation carrier from the indication of products of conception.

Qian YQ, Fu XY, Wang XQ, Luo YQ, Chen M, Yan K, Yang YM, Liu B, Wang LY, Huang YZ, Li HG, Pan HY, Jin F, Dong MY. Qian YQ, et al. Among authors: dong my. Mol Cytogenet. 2018 Jan 30;11:12. doi: 10.1186/s13039-018-0362-8. eCollection 2018. Mol Cytogenet. 2018. PMID: 29422950 Free PMC article.

8

Detection of fetal subchromosomal aberration with cell-free DNA screening led to diagnosis of parental translocation: Review of 11344 consecutive cases in a university hospital.

Qian YQ, Wang XQ, Chen M, Luo YQ, Yan K, Yang YM, Liu B, Wang LY, Huang YZ, Li HG, Pan HY, Jin F, Dong MY. Qian YQ, et al. Among authors: dong my. Eur J Med Genet. 2019 Feb;62(2):115-123. doi: 10.1016/j.ejmg.2018.06.012. Epub 2018 Jun 19. Eur J Med Genet. 2019. PMID: 29929010

9

Involvement of follistatin-like 3 in preeclampsia.

Xie J, Xu Y, Wan L, Wang P, Wang M, Dong M. Xie J, et al. Among authors: dong m. Biochem Biophys Res Commun. 2018 Nov 30;506(3):692-697. doi: 10.1016/j.bbrc.2018.10.139. Epub 2018 Oct 27. Biochem Biophys Res Commun. 2018. PMID: 30454705

10

The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies.

Li H, Lei Y, Zhu H, Luo Y, Qian Y, Chen M, Sun Y, Yan K, Yang Y, Liu B, Wang L, Huang Y, Hu J, Xu J, Dong M. Li H, et al. Among authors: dong m. Mol Cytogenet. 2018 Dec 3;11:59. doi: 10.1186/s13039-018-0407-z. eCollection 2018. Mol Cytogenet. 2018. PMID: 30524505 Free PMC article.

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