He DQ - Search Results

1

[Prenatal diagnosis of Thailand deletion of α-thalassemia 1 families].

Lin N, Lin Y, Huang HL, Lin XL, He DQ, He SQ, Guo DH, Li Y, Xu LP. Lin N, et al. Among authors: he sq, he dq. Zhonghua Yi Xue Za Zhi. 2016 Jun 28;96(24):1919-22. doi: 10.3760/cma.j.issn.0376-2491.2016.24.010. Zhonghua Yi Xue Za Zhi. 2016. PMID: 27373361 Chinese.

2

A new β-thalassemia deletion mutation [codon 36 (-C)] observed in a Chinese woman.

Huang H, Xu L, Lin N, Xu J, He D, Li Y, Zheng L, Liu H, Lin Y. Huang H, et al. Hemoglobin. 2010;34(6):599-603. doi: 10.3109/03630269.2010.526841. Hemoglobin. 2010. PMID: 21077770

3

Molecular spectrum of β-thalassemia in Fujian Province, Southeastern China.

Huang H, Xu L, Lin N, He D, Li Y, Guo D, Wang L, Wang Y, Zhen L, Xu J, Lin Y. Huang H, et al. Hemoglobin. 2013;37(4):343-50. doi: 10.3109/03630269.2013.792274. Epub 2013 May 20. Hemoglobin. 2013. PMID: 23682686

4

[Prenatal Diagnosis of A Case of SEA-HPFH Deletion Combined with Beta-Thalassemia in A Chinese Family].

Chen MH, Huang HL, Wang Y, Zhang M, Lin N, He DQ, Lin Y, Xu LP. Chen MH, et al. Among authors: he dq. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017 Aug;25(4):1142-1146. doi: 10.7534/j.issn.1009-2137.2017.04.032. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017. PMID: 28823283 Chinese.

5

[Prenatal diagnosis of a fetus with Miller-Dieker syndrome].

Xu L, Huang H, Wang Y, An G, Lin N, Zhang M, Wu X, He D, Chen M, Lin Y. Xu L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):879-883. doi: 10.3760/cma.j.issn.1003-9406.2017.06.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188621 Chinese.

6

Application of the BACs-on-Beads™ assay for rapid prenatal detection application of BoBs™ for PND of aneuploidies and microdeletions.

Huang H, Zhang M, Wang Y, Lin N, He D, Chen M, Chen L, Lin Y, Xu L. Huang H, et al. Mol Reprod Dev. 2018 Feb;85(2):146-154. doi: 10.1002/mrd.22945. Epub 2018 Jan 17. Mol Reprod Dev. 2018. PMID: 29247566

7

Optimization of regional median equations of prenatal screening markers for trisomy 21 in a Chinese population.

Xu L, Huang H, Zheng L, He D, Lin N, Wang L, Lin Y. Xu L, et al. Medicine (Baltimore). 2018 Aug;97(35):e12045. doi: 10.1097/MD.0000000000012045. Medicine (Baltimore). 2018. PMID: 30170416 Free PMC article.

8

Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China.

Huang H, Xu L, Chen M, Lin N, Xue H, Chen L, Wang Y, He D, Zhang M, Lin Y. Huang H, et al. Sci Rep. 2019 Mar 5;9(1):3493. doi: 10.1038/s41598-019-40089-5. Sci Rep. 2019. PMID: 30837609 Free PMC article.

9

[Prenatal diagnosis and clinical analysis of two fetuses with Cat-eye syndrome].

Wu X, An G, He D, Shen Q, Cai M, Huang H, Lin Y, Xu L. Wu X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 May 10;36(5):498-501. doi: 10.3760/cma.j.issn.1003-9406.2019.05.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31030443 Chinese.

10

Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age.

Wu X, An G, Xie X, Su L, Cai M, Chen X, Li Y, Lin N, He D, Wang M, Huang H, Xu L. Wu X, et al. J Clin Lab Anal. 2020 Apr;34(4):e23117. doi: 10.1002/jcla.23117. Epub 2019 Nov 24. J Clin Lab Anal. 2020. PMID: 31762079 Free PMC article.

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