Li DZ - Search Results

1

Improved outcomes in patients with prenatally detected 22q11.2 deletion syndrome.

Jing XY, Li DZ. Jing XY, et al. Among authors: li dz. Am J Obstet Gynecol. 2024 Apr;230(4):e49. doi: 10.1016/j.ajog.2023.11.1225. Epub 2023 Nov 10. Am J Obstet Gynecol. 2024. PMID: 37952869 No abstract available.

2

Prenatal diagnosis of 17q12 duplication and deletion syndrome in two fetuses with congenital anomalies.

Li R, Fu F, Zhang YL, Li DZ, Liao C. Li R, et al. Among authors: li dz. Taiwan J Obstet Gynecol. 2014 Dec;53(4):579-82. doi: 10.1016/j.tjog.2014.05.004. Taiwan J Obstet Gynecol. 2014. PMID: 25510704 Free article.

3

Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tract.

Lei TY, Fu F, Li R, Wang D, Wang RY, Jing XY, Deng Q, Li ZZ, Liu ZQ, Yang X, Li DZ, Liao C. Lei TY, et al. Among authors: li zz, li dz, li r. Nephrol Dial Transplant. 2017 Oct 1;32(10):1665-1675. doi: 10.1093/ndt/gfx031. Nephrol Dial Transplant. 2017. PMID: 28387813

4

[Application of chromosome microarray analysis in 489 children with developmental delay/intellectual disability].

Wang R, Lei T, Fu F, Li R, Jing X, Yang X, Pan M, Li D, Liao C. Wang R, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):528-533. doi: 10.3760/cma.j.issn.1003-9406.2017.04.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777852 Chinese.

5

NDUFA4 enhances neuron growth by triggering growth factors and inhibiting neuron apoptosis through Bcl-2 and cytochrome C mediated signaling pathway.

Fu F, Li Y, Li R, Lei TY, Wang D, Yang X, Han J, Pan M, Zhen L, Ou YM, Li J, Li FT, Jing XY, Li DZ, Liao C. Fu F, et al. Among authors: li ft, li y, li j, li dz, li r. Am J Transl Res. 2018 Jan 15;10(1):164-174. eCollection 2018. Am J Transl Res. 2018. PMID: 29423002 Free PMC article.

6

Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China.

Wang R, Lei T, Fu F, Li R, Jing X, Yang X, Liu J, Li D, Liao C. Wang R, et al. Pediatr Neonatol. 2019 Feb;60(1):35-42. doi: 10.1016/j.pedneo.2018.03.006. Epub 2018 Mar 26. Pediatr Neonatol. 2019. PMID: 29631977 Free article.

7

Pregnancy outcome of autosomal aneuploidies other than common trisomies detected by noninvasive prenatal testing in routine clinical practice.

Wan J, Li R, Zhang Y, Jing X, Yu Q, Li F, Li Y, Zhang L, Yi C, Li J, Li D, Liao C. Wan J, et al. Prenat Diagn. 2018 Oct;38(11):849-857. doi: 10.1002/pd.5340. Epub 2018 Sep 6. Prenat Diagn. 2018. PMID: 30078205

8

Prenatal diagnosis of 17q12 deletion syndrome: a retrospective case series.

Jing XY, Huang LY, Zhen L, Han J, Li DZ. Jing XY, et al. Among authors: li dz. J Obstet Gynaecol. 2019 Apr;39(3):323-327. doi: 10.1080/01443615.2018.1519693. Epub 2019 Jan 11. J Obstet Gynaecol. 2019. PMID: 30634886 Free article.

9

Confined placental trisomy detection through cell-free DNA in the maternal circulation: Benefit for pregnancy management.

Li DZ, He Y. Li DZ, et al. Am J Obstet Gynecol. 2019 Sep;221(3):286. doi: 10.1016/j.ajog.2019.05.030. Epub 2019 May 24. Am J Obstet Gynecol. 2019. PMID: 31132342 No abstract available.

10

Clinical utility of noninvasive prenatal screening for pathogenic copy number variants.

Xu LL, Li DZ. Xu LL, et al. Among authors: li dz. Am J Obstet Gynecol. 2019 Dec;221(6):660. doi: 10.1016/j.ajog.2019.08.030. Epub 2019 Aug 27. Am J Obstet Gynecol. 2019. PMID: 31469992 No abstract available.

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