Chen X - Search Results

1

Detection of four rare thalassemia variants using Single-molecule realtime sequencing.

Luo S, Chen X, Zeng D, Tang N, Yuan D, Liu B, Chen L, Zhong Q, Li J, Liu Y, Chen J, Wang X, Yan T. Luo S, et al. Among authors: chen j, chen l, chen x. Front Genet. 2022 Sep 2;13:974999. doi: 10.3389/fgene.2022.974999. eCollection 2022. Front Genet. 2022. PMID: 36159974 Free PMC article.

2

Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene HBA2: c.1A>G Mutation.

Chen X, Luo S, Huang J, Yuan D, Yan T, Cai R, Tang N. Chen X, et al. Hemoglobin. 2020 Jan;44(1):51-54. doi: 10.1080/03630269.2020.1711771. Epub 2020 Jan 14. Hemoglobin. 2020. PMID: 31933393

3

Analysis of rare thalassemia caused by HS-40 regulatory site deletion.

Luo S, Chen X, Zhong Q, Wang Q, Xu Z, Qin L, Wang J, Yuan D, Yan T, Tang N. Luo S, et al. Among authors: chen x. Hematology. 2020 Dec;25(1):286-291. doi: 10.1080/16078454.2020.1799587. Hematology. 2020. PMID: 32720864 Free article.

4

Analysis of Hb levels and degree of anemia in relation to genotype in 615 patients with hemoglobin H disease.

Luo S, Chen X, Chen L, Zhong Q, Wang Q, Xu Z, Huang J, Yan T, Tang N. Luo S, et al. Among authors: chen l, chen x. Expert Rev Hematol. 2020 Sep;13(9):1027-1033. doi: 10.1080/17474086.2020.1803736. Epub 2020 Aug 11. Expert Rev Hematol. 2020. PMID: 32727230

5

Pedigree Analysis of Nonhomologous Sequence Recombination of HBA1 and HBA2 Genes.

Luo SQ, Chen XY, Tang N, Huang J, Zhong QY, Cai R, Yan TZ. Luo SQ, et al. Hemoglobin. 2020 Sep;44(5):329-333. doi: 10.1080/03630269.2020.1807355. Epub 2020 Aug 19. Hemoglobin. 2020. PMID: 32811243

6

Application of Copy Number Variation Sequencing in Genetic Analysis of Miscarriages in Early and Middle Pregnancy.

Luo S, Chen X, Yan T, Ya J, Xu Z, Cai P, Yuan D, Tang N. Luo S, et al. Among authors: chen x. Cytogenet Genome Res. 2020;160(11-12):634-642. doi: 10.1159/000512801. Epub 2021 Mar 23. Cytogenet Genome Res. 2020. PMID: 33756471

7

The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation.

Luo S, Chen X, Zeng D, Tang N, Yuan D, Zhong Q, Mao A, Xu R, Yan T. Luo S, et al. Among authors: chen x. J Hum Genet. 2022 Apr;67(4):183-195. doi: 10.1038/s10038-021-00983-1. Epub 2021 Oct 25. J Hum Genet. 2022. PMID: 34690349 Free PMC article.

8

Correction to: The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation.

Luo S, Chen X, Zeng D, Tang N, Yuan D, Zhong Q, Mao A, Xu R, Yan T. Luo S, et al. Among authors: chen x. J Hum Genet. 2022 Apr;67(4):239-243. doi: 10.1038/s10038-021-00992-0. J Hum Genet. 2022. PMID: 34815527 Free PMC article. No abstract available.

9

[Cases Analysis of Hemoglobin H Disease Caused by HBA2:c.2T>C and HBA2:c.2delT Mutations].

Wang QH, Chen XY, Tang N, Yan TZ, Huang J, Zhong QY, Luo SQ. Wang QH, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2024 Apr;32(2):520-524. doi: 10.19746/j.cnki.issn.1009-2137.2024.02.030. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2024. PMID: 38660861 Chinese.

10

Genetic mutation analysis of hereditary spherocytosis in Guangxi Zhuang Autonomous Region.

Chen X, Liao L, Wu Y, Xiang L, Qin Y, Luo M, Lin F. Chen X, et al. J Hematop. 2023 Jun;16(2):95-101. doi: 10.1007/s12308-023-00545-8. Epub 2023 May 5. J Hematop. 2023. PMID: 38175446

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