Wang D - Search Results

1

Genetic tests aid in counseling of fetuses with cerebellar vermis defects.

Li L, Fu F, Li R, Xiao W, Yu Q, Wang D, Jing X, Zhang Y, Yang X, Pan M, Liu Z, Liao C. Li L, et al. Among authors: wang d. Prenat Diagn. 2020 Sep;40(10):1228-1238. doi: 10.1002/pd.5732. Epub 2020 May 28. Prenat Diagn. 2020. PMID: 32386258

2

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: wang d, wang ry. Nephrol Dial Transplant. 2017 Oct 1;32(10):1665-1675. doi: 10.1093/ndt/gfx031. Nephrol Dial Transplant. 2017. PMID: 28387813

3

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: wang d. Am J Transl Res. 2018 Jan 15;10(1):164-174. eCollection 2018. Am J Transl Res. 2018. PMID: 29423002 Free PMC article.

4

[Analysis of 26 fetuses with congenital anomalies of the kidney and urinary tract by whole exome sequencing].

Lei T, Fu F, Li R, Wang D, Yang D, Wang F, Yang X, Pan M, Zhen L, Han J, Li D, Liao C. Lei T, et al. Among authors: wang f, wang d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Dec 10;35(6):856-859. doi: 10.3760/cma.j.issn.1003-9406.2018.06.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30512163 Chinese.

5

Nonimmune hydrops fetalis: Genetic analysis and clinical outcome.

Deng Q, Fu F, Yu Q, Li R, Li F, Wang D, Lei T, Yang X, Liao C. Deng Q, et al. Among authors: wang d. Prenat Diagn. 2020 Jun;40(7):803-812. doi: 10.1002/pd.5691. Epub 2020 May 3. Prenat Diagn. 2020. PMID: 32267001

6

Prenatal exome sequencing in fetuses with congenital heart defects.

Li R, Fu F, Yu Q, Wang D, Jing X, Zhang Y, Li F, Li F, Han J, Pan M, Zhen L, Li D, Liao C. Li R, et al. Among authors: wang d. Clin Genet. 2020 Sep;98(3):215-230. doi: 10.1111/cge.13774. Epub 2020 Jun 9. Clin Genet. 2020. PMID: 32410215

7

Whole-exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography.

Lei TY, Fu F, Li R, Yu QX, Du K, Zhang WW, Deng Q, Li LS, Wang D, Yang X, Zhen L, Li DZ, Liao C. Lei TY, et al. Among authors: wang d. Prenat Diagn. 2020 Sep;40(10):1290-1299. doi: 10.1002/pd.5737. Epub 2020 Jul 15. Prenat Diagn. 2020. PMID: 32436246

8

Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease.

Fu F, Li R, Lei TY, Wang D, Yang X, Han J, Pan M, Zhen L, Li J, Li FT, Jing XY, Li DZ, Liao C. Fu F, et al. Among authors: wang d. Hum Genet. 2021 Feb;140(2):333-348. doi: 10.1007/s00439-020-02200-z. Epub 2020 Jul 21. Hum Genet. 2021. PMID: 32696347

9

A novel splicing mutation of ARHGAP29 is associated with nonsyndromic cleft lip with or without cleft palate.

Yu Q, Deng Q, Fu F, Li R, Zhang W, Wan J, Yang X, Wang D, Li F, Wu S, Li J, Li D, Liao C. Yu Q, et al. Among authors: wang d. J Matern Fetal Neonatal Med. 2022 Jul;35(13):2499-2506. doi: 10.1080/14767058.2020.1786523. Epub 2020 Jul 22. J Matern Fetal Neonatal Med. 2022. PMID: 32698641 Free article.

10

Microarray analysis in fetuses with duodenal obstruction: It is not just trisomy 21.

Zhang W, Lei T, Fu F, Deng Q, Li R, Wang D, Yang X, Li D, Liao C. Zhang W, et al. Among authors: wang d. Prenat Diagn. 2021 Feb;41(3):316-322. doi: 10.1002/pd.5834. Epub 2021 Jan 20. Prenat Diagn. 2021. PMID: 33000500

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