Yuan T - Search Results

1

[Diagnosis and prenatal diagnosis to a family of hemoglobin variant with α-thalassemia].

Du L, Wu J, Qin D, Wang J, Luo M, Guo H, Yuan T, Zhang Y, Wang Y, Yin A. Du L, et al. Among authors: yuan t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Apr;32(2):226-8. doi: 10.3760/cma.j.issn.1003-9406.2015.02.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25863092 Chinese.

2

[Value of Analyzing Hemoglobin A₂ by ROC Curve for Screening Thalassemia].

He TW, Yu LH, Guo H, Wang YX, DU L, Yuan TL, Zhang YX, Luo MY, Yin AH. He TW, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016 Dec;24(6):1828-1832. doi: 10.7534/j.issn.1009-2137.2016.06.038. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016. PMID: 28024502 Chinese.

3

[Gene Diagnosis and Phenotypic Analysis of β-Thalassemia Caused from a Rare Synonymous Mutation CD29 (C>T)].

Qin DQ, DU L, Ding HK, Wang JC, Yuan TL, Yao CZ, Lan FF. Qin DQ, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Apr;28(2):577-582. doi: 10.19746/j.cnki.issn.1009-2137.2020.02.037. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020. PMID: 32319399 Chinese.

4

[Hematological Analysis and Diagnosis of Two Rare Abnormal Hemoglobin].

Wang JC, Guo H, Huang HJ, Yuan TL, Yao CZ, Qin DQ, DU L. Wang JC, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Dec;28(6):2028-2032. doi: 10.19746/j.cnki.issn.1009-2137.2020.06.038. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020. PMID: 33283737 Chinese.

5

[Differential Diagnosis of Three Commonest Deletion β-Thalassemia in Chinese].

Wang JC, Yao CZ, Huang YL, Liu L, Yuan TL, Qin DQ. Wang JC, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021 Aug;29(4):1247-1250. doi: 10.19746/j.cnki.issn.1009-2137.2021.04.035. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021. PMID: 34362510 Chinese.

6

[Genetic Effect Analysis of β-globin Gene 3'UTR+101G>C (HBB:c. *233G>C) Variant].

DU L, Yao CZ, Bao XQ, Liang J, Yuan TL, Qin DQ, Wang JC. DU L, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021 Aug;29(4):1271-1274. doi: 10.19746/j.cnki.issn.1009-2137.2021.04.040. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021. PMID: 34362515 Chinese.

7

[Molecular and prenatal diagnosis of a rare mutation IVS1-116（A→G）of α2-globin gene].

Qin D, Wang J, Yu L, Yuan T, Zhang Y, Wang Y, Luo M, Liang J, Du L. Qin D, et al. Among authors: yuan t. Zhonghua Xue Ye Xue Za Zhi. 2015 Sep;36(9):791-2. doi: 10.3760/cma.j.issn.0253-2727.2015.09.016. Zhonghua Xue Ye Xue Za Zhi. 2015. PMID: 26462784 Free PMC article. Chinese. No abstract available.

8

Genetic and phenotypic analysis of a rare asymptomatic case of a homozygous Chinese ^Gγ⁺(^Aγδβ)⁰-thalassemia deletion in a Chinese family.

Du L, Qin D, Wang J, Yu L, Yao C, Liu L, Zhang Y, Hu T, Yuan T, Liang J, Yin A. Du L, et al. Among authors: yuan t. Clin Biochem. 2020 Feb;76:11-16. doi: 10.1016/j.clinbiochem.2019.11.003. Epub 2019 Nov 22. Clin Biochem. 2020. PMID: 31765637

9

Compound heterozygosity for hemoglobin variant Hb-Broomhill and the Southeast Asian α-thalassemia deletion does not worsen outcome: a case report of two unrelated patients.

Qin D, Du L, Wang J, Yao C, Guo H, Yuan T, Liang J, Yin A. Qin D, et al. Among authors: yuan t. J Int Med Res. 2020 Nov;48(11):300060520967825. doi: 10.1177/0300060520967825. J Int Med Res. 2020. PMID: 33213249 Free PMC article.

10

The first Chinese case of unstable Hemoglobin Santa Ana detected by capillary electrophoresis: a case report and literature review.

Du L, Qin D, Wang J, Yao C, Zhu J, Guo H, Yuan T, Liang J, Yin A. Du L, et al. Among authors: yuan t. Hematology. 2022 Dec;27(1):258-262. doi: 10.1080/16078454.2022.2035049. Hematology. 2022. PMID: 35192774 Free article. Review.

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