Wu Q - Search Results

1

Diagnosis of fetal osteogenesis imperfecta by multidisciplinary assessment: a retrospective study of 10 cases.

Wu Q, Wang W, Cao L, Sun L, Xu Y, Zhong X. Wu Q, et al. Fetal Pediatr Pathol. 2015 Feb;34(1):57-64. doi: 10.3109/15513815.2014.962198. Epub 2014 Oct 7. Fetal Pediatr Pathol. 2015. PMID: 25289482

2

Investigation of the frequencies of prenatally diagnosed fetal chromosomal abnormalities at a single institution.

Wu Q, Wang W, Kong H, Sun L, Ge Y, Xu Y, Zhou Y. Wu Q, et al. Fetal Pediatr Pathol. 2013 Jun;32(3):163-8. doi: 10.3109/15513815.2012.684847. Epub 2012 May 18. Fetal Pediatr Pathol. 2013. PMID: 22607389

3

Diagnosis of Prenatal-Onset Achondrogenesis Type II by a Multidisciplinary Assessment: A Retrospective Study of 2 Cases.

Wang W, Wu Q, Sun L, Zhong X, Xu Y, Xie X, Su Z. Wang W, et al. Among authors: wu q. Case Rep Obstet Gynecol. 2019 Jul 17;2019:7981767. doi: 10.1155/2019/7981767. eCollection 2019. Case Rep Obstet Gynecol. 2019. PMID: 31392067 Free PMC article.

4

Mutation Analysis of COL1A1 and COL1A2 in Fetuses with Osteogenesis Imperfecta Type II/III.

Wang W, Wu Q, Cao L, Sun L, Xu Y, Guo Q. Wang W, et al. Among authors: wu q. Gynecol Obstet Invest. 2020;85(2):149-152. doi: 10.1159/000370196. Epub 2015 Jan 27. Gynecol Obstet Invest. 2020. Retraction in: Gynecol Obstet Invest. 2020;85(5):446. doi: 10.1159/000511941 PMID: 25633413 Retracted.

5

[Diagnosis of a fetus with X-linked hydrocephalus due to mutation of L1CAM gene].

Wu Q, Sun L, Xu Y, Yang X, Sun S, Wang W. Wu Q, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Sep 10;36(9):897-900. doi: 10.3760/cma.j.issn.1003-9406.2019.09.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31515785 Chinese.

6

Prenatal diagnosis of familial recessive PIGN mutation associated with multiple anomalies: A case report.

Sun L, Yang X, Xu Y, Sun S, Wu Q. Sun L, et al. Among authors: wu q. Taiwan J Obstet Gynecol. 2021 May;60(3):530-533. doi: 10.1016/j.tjog.2021.03.026. Taiwan J Obstet Gynecol. 2021. PMID: 33966742 Free article.

7

Rapid prenatal diagnosis of common numerical chromosomal abnormalities by high-resolution melting analysis of segmental duplications.

Zhou Y, Xiao L, Wu Q, Zhang K, Guo Q. Zhou Y, et al. Among authors: wu q. Genet Test Mol Biomarkers. 2014 Mar;18(3):141-8. doi: 10.1089/gtmb.2013.0373. Epub 2013 Dec 9. Genet Test Mol Biomarkers. 2014. PMID: 24321085

8

[Clinical application of real-time PCR for the detection of genetic mutations underlying spinal muscular atrophy].

Jiang Y, Peng G, Wu Q, Zhou Y. Jiang Y, et al. Among authors: wu q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Apr;31(2):180-4. doi: 10.3760/cma.j.issn.1003-9406.2014.02.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24711027 Chinese.

9

The role of DNA methylation in syndromic and non-syndromic congenital heart disease.

Cao J, Wu Q, Huang Y, Wang L, Su Z, Ye H. Cao J, et al. Among authors: wu q. Clin Epigenetics. 2021 Apr 26;13(1):93. doi: 10.1186/s13148-021-01077-7. Clin Epigenetics. 2021. PMID: 33902696 Free PMC article. Review.

10

Meta-analysis: association of homocysteine with recurrent spontaneous abortion.

Li J, Feng D, He S, Wu Q, Su Z, Ye H. Li J, et al. Among authors: wu q. Women Health. 2021 Aug;61(7):713-720. doi: 10.1080/03630242.2021.1957747. Epub 2021 Aug 1. Women Health. 2021. PMID: 34334120 Review.

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