Han X - Search Results

1

Prenatal Diagnosis of Chromosomal Mosaicism in Over 18,000 Pregnancies: A Five-Year Single-Tertiary-Center Retrospective Analysis.

Li S, Shi Y, Han X, Chen Y, Shen Y, Hu W, Zhao X, Wang Y. Li S, et al. Among authors: han x. Front Genet. 2022 May 16;13:876887. doi: 10.3389/fgene.2022.876887. eCollection 2022. Front Genet. 2022. PMID: 35651933 Free PMC article.

2

Two cases of placental T21 mosaicism: challenging the detection limits of non-invasive prenatal testing.

Wang Y, Zhu J, Chen Y, Lu S, Chen B, Zhao X, Wu Y, Han X, Ma D, Liu Z, Cram D, Cheng W. Wang Y, et al. Among authors: han x. Prenat Diagn. 2013 Dec;33(12):1207-10. doi: 10.1002/pd.4212. Epub 2013 Aug 31. Prenat Diagn. 2013. PMID: 23929588 No abstract available.

3

Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.

Wang Y, Chen Y, Tian F, Zhang J, Song Z, Wu Y, Han X, Hu W, Ma D, Cram D, Cheng W. Wang Y, et al. Among authors: han x. Clin Chem. 2014 Jan;60(1):251-9. doi: 10.1373/clinchem.2013.215145. Epub 2013 Nov 5. Clin Chem. 2014. PMID: 24193117

4

A genotype-phenotype correlation study reveals that a non-coding RNA might be associated with cardiovascular anomalies in fetuses with WHS.

Wu Y, Tao J, Wang YL, Hu WJ, Han X, Cheng WW. Wu Y, et al. Among authors: han x. Prenat Diagn. 2016 Oct;36(10):979-981. doi: 10.1002/pd.4884. Epub 2016 Aug 19. Prenat Diagn. 2016. PMID: 27501084 No abstract available.

5

The clinical use of chromosomal microarray analysis in detection of fetal chromosomal rearrangements: a study from China Mainland.

Wu Y, Wang Y, Tao J, Han X, Zhao X, Liu C, Gao L, Cheng W. Wu Y, et al. Among authors: han x. Eur J Obstet Gynecol Reprod Biol. 2017 May;212:44-50. doi: 10.1016/j.ejogrb.2017.03.007. Epub 2017 Mar 7. Eur J Obstet Gynecol Reprod Biol. 2017. PMID: 28340467

6

Molecular and Cytogenetic Characterization of a Fetus with Mosaic Ring Chromosome 13: A Very Rare Case.

Zhao XR, Han X, Wang YL, Hu WJ. Zhao XR, et al. Among authors: han x. Chin Med J (Engl). 2017 Dec 20;130(24):3007-3008. doi: 10.4103/0366-6999.220308. Chin Med J (Engl). 2017. PMID: 29237938 Free PMC article. No abstract available.

7

Chromosomal microarray analysis in fetuses with congenital anomalies of the kidney and urinary tract: A prospective cohort study and meta-analysis.

Li S, Han X, Wang Y, Chen S, Niu J, Qian Z, Li P, Jin L, Xu C. Li S, et al. Among authors: han x. Prenat Diagn. 2019 Feb;39(3):165-174. doi: 10.1002/pd.5420. Epub 2019 Feb 7. Prenat Diagn. 2019. PMID: 30650192

8

Prenatal Diagnosis of Microdeletions or Microduplications in the Proximal, Central, and Distal Regions of Chromosome 22q11.2: Ultrasound Findings and Pregnancy Outcome.

Li S, Han X, Ye M, Chen S, Shen Y, Niu J, Wang Y, Xu C. Li S, et al. Among authors: han x. Front Genet. 2019 Aug 30;10:813. doi: 10.3389/fgene.2019.00813. eCollection 2019. Front Genet. 2019. PMID: 31543904 Free PMC article.

9

Should chromosomal microarray be offered to fetuses with ultrasonographic soft markers in second trimester: A prospective cohort study and meta-analysis.

Li S, Han X, Ye M, Chen S, Shen Y, Niu J, Wang Y, Xu C. Li S, et al. Among authors: han x. Prenat Diagn. 2020 Dec;40(12):1569-1577. doi: 10.1002/pd.5815. Epub 2020 Aug 31. Prenat Diagn. 2020. PMID: 32812229

10

A rare cardiac phenotype of dextrocardia observed in a fetus with 1p36 deletion syndrome and a balanced translocation: a prenatal case report.

Gao L, Zhang J, Han X, Hu W, Sun J, Tan Y, Zhao X, Hua R, Wang S, Zhang Y, Wang Y, Wu Y. Gao L, et al. Among authors: han x. Mol Cytogenet. 2020 Nov 16;13(1):48. doi: 10.1186/s13039-020-00514-1. Mol Cytogenet. 2020. PMID: 33292381 Free PMC article.

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