Meng L - Search Results

1

Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study.

Wang Y, Cheng Q, Meng L, Luo C, Hu H, Zhang J, Cheng J, Xu T, Jiang T, Liang D, Hu P, Xu Z. Wang Y, et al. Among authors: meng l. Clin Genet. 2017 Jun;91(6):849-858. doi: 10.1111/cge.12926. Epub 2016 Dec 22. Clin Genet. 2017. PMID: 27883173

2

Coagulation and prothrombotic state parameters: a clinical analysis during early pregnancy.

Chen H, Zhou L, Meng L, Liu M, Tan J, Gao L, Zhang J. Chen H, et al. Among authors: meng l. Ir J Med Sci. 2011 Dec;180(4):813-7. doi: 10.1007/s11845-011-0737-x. Epub 2011 Aug 2. Ir J Med Sci. 2011. PMID: 21809018

3

Long-term cultured mesenchymal stem cells frequently develop genomic mutations but do not undergo malignant transformation.

Wang Y, Zhang Z, Chi Y, Zhang Q, Xu F, Yang Z, Meng L, Yang S, Yan S, Mao A, Zhang J, Yang Y, Wang S, Cui J, Liang L, Ji Y, Han ZB, Fang X, Han ZC. Wang Y, et al. Among authors: meng l. Cell Death Dis. 2013 Dec 5;4(12):e950. doi: 10.1038/cddis.2013.480. Cell Death Dis. 2013. PMID: 24309937 Free PMC article.

4

Characteristics of immune cell changes before and after immunotherapy and their clinical significance in patients with unexplained recurrent spontaneous abortion.

Gao L, Zhang JP, Chen H, Zhang SN, Chen LB, Tan JP, Liu ML, Meng LL, Wang YH, Zhang R, Liu YL, Cai WB. Gao L, et al. Among authors: meng ll. Genet Mol Res. 2014 Feb 27;13(1):1169-78. doi: 10.4238/2014.February.27.1. Genet Mol Res. 2014. PMID: 24634173 Free article.

5

Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach.

Dong Z, Zhang J, Hu P, Chen H, Xu J, Tian Q, Meng L, Ye Y, Wang J, Zhang M, Li Y, Wang H, Yu S, Chen F, Xie J, Jiang H, Wang W, Choy KW, Xu Z. Dong Z, et al. Among authors: meng l. Genet Med. 2016 Sep;18(9):940-8. doi: 10.1038/gim.2015.199. Epub 2016 Jan 28. Genet Med. 2016. PMID: 26820068 Free article.

6

Clinical application of whole-genome low-coverage next-generation sequencing to detect and characterize balanced chromosomal translocations.

Liang D, Wang Y, Ji X, Hu H, Zhang J, Meng L, Lin Y, Ma D, Jiang T, Jiang H, Asan, Song L, Guo J, Hu P, Xu Z. Liang D, et al. Among authors: meng l. Clin Genet. 2017 Apr;91(4):605-610. doi: 10.1111/cge.12844. Epub 2016 Sep 5. Clin Genet. 2017. PMID: 27491356

7

Clinical application of targeted next-generation sequencing in fetuses with congenital heart defect.

Hu P, Qiao F, Wang Y, Meng L, Ji X, Luo C, Xu T, Zhou R, Zhang J, Yu B, Wang L, Wang T, Pan Q, Ma D, Liang D, Xu Z. Hu P, et al. Among authors: meng l. Ultrasound Obstet Gynecol. 2018 Aug;52(2):205-211. doi: 10.1002/uog.19042. Epub 2018 Jun 25. Ultrasound Obstet Gynecol. 2018. PMID: 29536580 Free article.

8

[Association between interleukin-17A and 17F single nucleotide polymorphisms and knee osteoarthritis].

Zhang PL, Yang FM, Qiao ZZ, Liu J, Yang QY, Wang YJ, Qi M, Cui LN, Meng L, Li XP. Zhang PL, et al. Among authors: meng l. Zhonghua Yi Xue Za Zhi. 2019 Jun 25;99(24):1870-1874. doi: 10.3760/cma.j.issn.0376-2491.2019.24.007. Zhonghua Yi Xue Za Zhi. 2019. PMID: 31269582 Chinese.

9

Systematic analysis of copy-number variations associated with early pregnancy loss.

Wang Y, Li Y, Chen Y, Zhou R, Sang Z, Meng L, Tan J, Qiao F, Bao Q, Luo D, Peng C, Wang YS, Luo C, Hu P, Xu Z. Wang Y, et al. Among authors: meng l. Ultrasound Obstet Gynecol. 2020 Jan;55(1):96-104. doi: 10.1002/uog.20412. Ultrasound Obstet Gynecol. 2020. PMID: 31364215 Free article.

10

Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect.

Qiao F, Wang Y, Zhang C, Zhou R, Wu Y, Wang C, Meng L, Mao P, Cheng Q, Luo C, Hu P, Xu Z. Qiao F, et al. Among authors: meng l. Ultrasound Obstet Gynecol. 2021 Sep;58(3):377-387. doi: 10.1002/uog.23532. Ultrasound Obstet Gynecol. 2021. PMID: 33142350 Free article.

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