Li Y - Search Results

1

A cross-sectional survey of pregnant women's knowledge of chromosomal aneuploidy and microdeletion and microduplication syndromes.

Yang J, Chen M, Ye X, Chen F, Li Y, Li N, Wu W, Sun J. Yang J, et al. Among authors: li y, li n. Eur J Obstet Gynecol Reprod Biol. 2021 Jan;256:82-90. doi: 10.1016/j.ejogrb.2020.10.001. Epub 2020 Nov 3. Eur J Obstet Gynecol Reprod Biol. 2021. PMID: 33176246

2

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. 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.

3

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: li s, li y, li n. Prenat Diagn. 2019 Dec;39(13):1273-1282. doi: 10.1002/pd.5597. Epub 2019 Nov 11. Prenat Diagn. 2019. PMID: 31671222

4

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: li y. Prenat Diagn. 2020 Jul;40(8):918-924. doi: 10.1002/pd.5641. Epub 2020 Jun 4. Prenat Diagn. 2020. PMID: 31916613

5

Clinical application of medical exome sequencing for prenatal diagnosis of fetal structural anomalies.

Chen M, Chen J, Wang C, Chen F, Xie Y, Li Y, Li N, Wang J, Zhang VW, Chen D. Chen M, et al. Among authors: li y, li n. Eur J Obstet Gynecol Reprod Biol. 2020 Aug;251:119-124. doi: 10.1016/j.ejogrb.2020.04.033. Epub 2020 May 20. Eur J Obstet Gynecol Reprod Biol. 2020. PMID: 32502767

6

An induced pluripotent stem cell line (GZHMCi003-A) derived from a fetus with exon 3 heterozygous deletion in RUNX2 gene causing cleidocranial dysplasia.

Chen M, Lin SM, Li N, Li Y, Li Y, Zhang L. Chen M, et al. Among authors: li y, li n. Stem Cell Res. 2021 Mar;51:102166. doi: 10.1016/j.scr.2021.102166. Epub 2021 Jan 9. Stem Cell Res. 2021. PMID: 33477036 Free article.

7

Noninvasive prenatal testing for β-thalassemia by targeted nanopore sequencing combined with relative haplotype dosage (RHDO): a feasibility study.

Jiang F, Liu W, Zhang L, Guo Y, Chen M, Zeng X, Wang Y, Li Y, Xian J, Du B, Xie Y, Ouyang S, Li S, Yang Y, Zhang C, Luo F, Sun X. Jiang F, et al. Among authors: li s, li y. Sci Rep. 2021 Mar 11;11(1):5714. doi: 10.1038/s41598-021-85128-2. Sci Rep. 2021. PMID: 33707551 Free PMC article.

8

The application of late amniocentesis: a retrospective study in a tertiary fetal medicine center in China.

Li Y, Yan H, Chen J, Chen F, Jian W, Wang J, Ye X, Li Y, Li N, Chiu PCN, Chen M. Li Y, et al. Among authors: li n. BMC Pregnancy Childbirth. 2021 Mar 30;21(1):266. doi: 10.1186/s12884-021-03723-7. BMC Pregnancy Childbirth. 2021. PMID: 33784964 Free PMC article.

9

Selective termination of the fetus in multiple pregnancies using ultrasound-guided radiofrequency ablation.

Li N, Sun J, Wang J, Jian W, Lu J, Miao Y, Li Y, Chen F, Chen D, Ye X, Chen M. Li N, et al. Among authors: li y. BMC Pregnancy Childbirth. 2021 Dec 10;21(1):821. doi: 10.1186/s12884-021-04285-4. BMC Pregnancy Childbirth. 2021. PMID: 34893028 Free PMC article.

10

Prenatal diagnosis of Noonan syndrome in a set of monozygotic twins- a case report.

Jian W, Yuan H, Liu Y, Sun J, Chen F, Li Y, Chen M. Jian W, et al. Among authors: li y. BMC Pregnancy Childbirth. 2023 Jan 6;23(1):10. doi: 10.1186/s12884-022-05323-5. BMC Pregnancy Childbirth. 2023. PMID: 36609239 Free PMC article.

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