Xie Y - Search Results

1

Molecular Characterization Analysis of Thalassemia and Hemoglobinopathy in Quanzhou, Southeast China: A Large-Scale Retrospective Study.

Zhuang J, Zhang N, Wang Y, Zhang H, Zheng Y, Jiang Y, Xie Y, Chen D. Zhuang J, et al. Among authors: xie y. Front Genet. 2021 Sep 30;12:727233. doi: 10.3389/fgene.2021.727233. eCollection 2021. Front Genet. 2021. PMID: 34659349 Free PMC article.

2

The 46, XX Ovotesticular Disorder of Sex Development With Xq27.1q27.2 Duplication Involving the SOX3 Gene: A Rare Case Report and Literature Review.

Zhuang J, Chen C, Li J, Jiang Y, Wang J, Wang Y, Zeng S, Lin Y, Xie Y. Zhuang J, et al. Among authors: xie y. Front Pediatr. 2021 Jun 11;9:682846. doi: 10.3389/fped.2021.682846. eCollection 2021. Front Pediatr. 2021. PMID: 34178900 Free PMC article.

3

Cytogenetic and molecular analysis of distal 4q duplication with distinctive phenotype using single-nucleotide polymorphism array.

Zhuang J, Zhang N, Fu W, Yao J, Li Y, Zeng S, Wang Y, Xie Y, Jiang Y. Zhuang J, et al. Among authors: xie y. Mol Cytogenet. 2021 Sep 29;14(1):46. doi: 10.1186/s13039-021-00568-9. Mol Cytogenet. 2021. PMID: 34587985 Free PMC article.

4

The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis.

Chen Y, Xie Y, Jiang Y, Luo Q, Shi L, Zeng S, Zhuang J, Lyu G. Chen Y, et al. Among authors: xie y. Front Pediatr. 2021 Oct 15;9:743639. doi: 10.3389/fped.2021.743639. eCollection 2021. Front Pediatr. 2021. PMID: 34722424 Free PMC article.

5

Effective Identification of Maternal Malignancies in Pregnancies Undergoing Noninvasive Prenatal Testing.

Li J, Ju J, Zhao Q, Liu W, Yuan Y, Liu Q, Zhou L, Han Y, Yuan W, Huang Y, Xie Y, Li Z, Chen J, Huang S, Chen R, Li W, Tan M, Wang D, Zhou S, Zhang J, Zeng F, Yu N, Su F, Chen M, Ge Y, Huang Y, Jin X. Li J, et al. Among authors: xie y. Front Genet. 2022 Feb 10;13:802865. doi: 10.3389/fgene.2022.802865. eCollection 2022. Front Genet. 2022. PMID: 35265103 Free PMC article.

6

Complex Chromosomal Rearrangement Causes Male Azoospermia: A Case Report and Literature Review.

Liang Y, Xie Y, Kong S, Pan Q, Qiu W, Wang D, Li M, Lin S, Liu Z, Sun X. Liang Y, et al. Among authors: xie y. Front Genet. 2022 Feb 24;13:792539. doi: 10.3389/fgene.2022.792539. eCollection 2022. Front Genet. 2022. PMID: 35281846 Free PMC article.

7

Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing.

Zhuang J, Chen C, Chen Y, Zeng S, Jiang Y, Wang Y, Chen X, Xie Y, Wang G. Zhuang J, et al. Among authors: xie y. Front Genet. 2022 Mar 25;13:829613. doi: 10.3389/fgene.2022.829613. eCollection 2022. Front Genet. 2022. PMID: 35401667 Free PMC article.

8

Identification of a Rare Variant of c.1777G>A (p.G593S) in the COL1A1 Gene as the Etiology of Recurrent Osteogenesis Imperfecta by Whole-Exome Sequencing.

Zhuang J, Chen C, Chen Y, Luo Q, Wang Y, Jiang Y, Zeng S, Xie Y, Chen D. Zhuang J, et al. Among authors: xie y. Front Pediatr. 2022 Apr 8;10:816090. doi: 10.3389/fped.2022.816090. eCollection 2022. Front Pediatr. 2022. PMID: 35463886 Free PMC article.

9

Third-Generation Sequencing as a New Comprehensive Technology for Identifying Rare α- and β-Globin Gene Variants in Thalassemia Alleles in the Chinese Population.

Zhuang J, Chen C, Fu W, Wang Y, Zhuang Q, Lu Y, Xie T, Xu R, Zeng S, Jiang Y, Xie Y, Wang G. Zhuang J, et al. Among authors: xie y, xie t. Arch Pathol Lab Med. 2023 Feb 1;147(2):208-214. doi: 10.5858/arpa.2021-0510-OA. Arch Pathol Lab Med. 2023. PMID: 35639603 Free article.

10

Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese population.

Zhuang J, Chen C, Huang R, Luo Q, Jiang Y, Zeng S, Wang Y, Xie Y. Zhuang J, et al. Among authors: xie y. Mol Cytogenet. 2022 Jun 7;15(1):22. doi: 10.1186/s13039-022-00599-w. Mol Cytogenet. 2022. PMID: 35672790 Free PMC article.

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