Huang HL - Search Results

1

[Gene Diagnosis and Analysis of Clinical Hematological Phenotype of Thailand Deleted α-Thalassemia 1].

Lin N, Huang HL, Wang Y, Zheng L, Fang XQ, Cai MY, Wang LS, Liu HK, Xu LP, Lin Y. Lin N, et al. Among authors: huang hl. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016 Aug;24(4):1116-20. doi: 10.7534/j.issn.1009-2137.2016.04.029. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016. PMID: 27531785 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

Quadruplex real-time polymerase chain reaction assay for molecular diagnosis of Y-chromosomal microdeletions.

Guo Q, Lan F, Xu L, Jiang Y, Xiao L, Huang H, Zhou Y. Guo Q, et al. Fertil Steril. 2012 Apr;97(4):864-9. doi: 10.1016/j.fertnstert.2012.01.088. Epub 2012 Jan 23. Fertil Steril. 2012. PMID: 22270555 Free article.

4

[Relationship between gene polymorphism of GABAA receptors gene and childhood autism].

Lu GB, Ou P, Xu LP, Huang HL, Cheng L, Yang SW, Qian QF, Huang Y, Xie YQ, Yu QJ, Wang ZQ, Lin Y. Lu GB, et al. Among authors: huang hl, huang y. Zhonghua Yu Fang Yi Xue Za Zhi. 2012 May;46(5):460-4. Zhonghua Yu Fang Yi Xue Za Zhi. 2012. PMID: 22883737 Chinese.

5

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

6

[Molecular epidemiological analysis of α- and β-thalassemia in Fujian province].

Xu LP, Huang HL, Wang Y, Zheng L, Wang LS, Xu JB, Huang XX, Lin Y. Xu LP, et al. Among authors: huang hl, huang xx. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Aug;30(4):403-6. doi: 10.3760/cma.j.issn.1003-9406.2013.04.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23926004 Chinese.

7

[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: huang hl. 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.

8

[Prenatal diagnosis of 22q11 microdeletion syndrome].

Cai M, Huang H, Lin N, Guo N, Wu X, Su L, Xu L. Cai M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):192-195. doi: 10.3760/cma.j.issn.1003-9406.2017.02.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397216 Chinese.

9

[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: huang hl. 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.

10

[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.

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