Qin D - Search Results

1

Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C).

Du L, Bao X, He W, Qin D, Wang J, Xiong Y, Shi X, Ding H, Yao C, Wu J. Du L, et al. Among authors: qin d. J Int Med Res. 2021 Jul;49(7):3000605211031429. doi: 10.1177/03000605211031429. J Int Med Res. 2021. PMID: 34334003 Free PMC article.

2

Development of bead-based suspension array technology for the diagnosis of thalassemia.

Yin A, Zhang L, Luo M, He T, Zhang Y, Liu C, Du L, Qin D, Liang J, Li B, Wu L, Ma Y, Guo H, Wang J, Yuan T, Wang Y, Zhang Y, Zhang X. Yin A, et al. Among authors: qin d. Am J Hematol. 2014 Dec;89(12):1158-9. doi: 10.1002/ajh.23830. Am J Hematol. 2014. PMID: 25118110 Free article. No abstract available.

3

[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: qin d. 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.

4

[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. 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.

5

[Genetic Analysis, Prenatal Diagnosis and Preimplantation Genetic Diagnosis of Taiwanese Deletion β-Thalassemia].

DU L, Qin DQ, Liu L, Lu J, Yao CZ, Huang HJ, Wang JC. DU L, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019 Oct;27(5):1585-1591. doi: 10.19746/j.cnki.issn.1009-2137.2019.05.034. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019. PMID: 31607316 Chinese.

6

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: qin d. Clin Biochem. 2020 Feb;76:11-16. doi: 10.1016/j.clinbiochem.2019.11.003. Epub 2019 Nov 22. Clin Biochem. 2020. PMID: 31765637

7

[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.

8

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. J Int Med Res. 2020 Nov;48(11):300060520967825. doi: 10.1177/0300060520967825. J Int Med Res. 2020. PMID: 33213249 Free PMC article.

9

[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.

10

Comparison of cord blood hematological parameters among normal, α-thalassemia, and β-thalassemia fetuses between 17 and 38 weeks of gestation.

Zhan W, Guo H, Hu S, Wang J, Qin D, Liang J, Du L, Luo M. Zhan W, et al. Among authors: qin d. Sci Rep. 2021 Feb 15;11(1):3844. doi: 10.1038/s41598-021-82297-y. Sci Rep. 2021. PMID: 33589684 Free PMC article.

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