He Y - Search Results

1

A new partial trisomy 12p with artery catheter vagus, congenital cataracts, external auditory canal, and no turbinate.

Liu YH, Xie RG, Zhang XY, Wei SD, He Y, Xu WF, Lin YY, Xiong F. Liu YH, et al. Among authors: he y. Gene. 2012 Nov 1;509(1):164-7. doi: 10.1016/j.gene.2012.07.052. Epub 2012 Aug 8. Gene. 2012. PMID: 22959136

2

Detection of Hb anti-Lepore Hong Kong (NG_000007.3: g.63154_70565dup) in Chinese individuals.

Lou JW, He Y, Liu YH, Zhong BM, Zhao Y, He XX, Li DZ. Lou JW, et al. Among authors: he xx, he y. Hemoglobin. 2014;38(2):146-8. doi: 10.3109/03630269.2013.875477. Epub 2014 Jan 29. Hemoglobin. 2014. PMID: 24471736

3

Screening and diagnosis of Hb Quong Sze [HBA2: c.377T > C (or HBA1)] in a prenatal control program for thalassemia.

Yang Y, Lou JW, Liu YH, He Y, Li DZ. Yang Y, et al. Among authors: he y. Hemoglobin. 2014;38(3):158-60. doi: 10.3109/03630269.2014.910669. Hemoglobin. 2014. PMID: 24826791

4

Delineation of the molecular basis of borderline hemoglobin A2 in Chinese individuals.

Lou JW, Li DZ, Zhang Y, He Y, Sun MN, Ye WL, Liu YH. Lou JW, et al. Among authors: he y. Blood Cells Mol Dis. 2014 Dec;53(4):261-4. doi: 10.1016/j.bcmd.2014.04.005. Epub 2014 May 21. Blood Cells Mol Dis. 2014. PMID: 24857170

5

Prevalence and molecular characterization of structural hemoglobin variants in the Dongguan region of Guangdong province, southern China.

Lou JW, Wang T, Liu YH, He Y, Zhong BM, Liu JX, Zhao Y, Ye WL, Li DZ. Lou JW, et al. Among authors: he y. Hemoglobin. 2014;38(4):282-6. doi: 10.3109/03630269.2014.928779. Epub 2014 Jul 2. Hemoglobin. 2014. PMID: 24985555

6

[Application of noninvasive fetal trisomy testing based on massively parallel sequencing for the detection of chromosomal deletions and duplications].

Wen S, Wei F, He Y, Xu W, Xie R, Zhang X, Liu Y, Xiong F. Wen S, et al. Among authors: he y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Oct;31(5):557-60. doi: 10.3760/cma.j.issn.1003-9406.2014.01.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25297580 Chinese.

7

Rapid detection of α-thalassaemia alleles of --(SEA)/, -α(3.7)/ and -α(4.2)/ using a dual labelling, self-quenching hybridization probe/melting curve analysis.

Gao L, Liu Y, Sun M, Zhao Y, Xie R, He Y, Xu W, Liu J, Lin Y, Lou J. Gao L, et al. Among authors: he y. Mol Cell Probes. 2015 Dec;29(6):438-441. doi: 10.1016/j.mcp.2015.07.004. Epub 2015 Jul 17. Mol Cell Probes. 2015. PMID: 26190814

8

Fetal Anemia and Hydrops Fetalis Associated with Homozygous Hb Constant Spring (HBA2: c.427T > C).

He Y, Zhao Y, Lou JW, Liu YH, Li DZ. He Y, et al. Hemoglobin. 2016;40(2):97-101. doi: 10.3109/03630269.2015.1126721. Epub 2016 Jan 13. Hemoglobin. 2016. PMID: 26757782

9

A prenatal case of osteogenesis imperfecta diagnosed with next-generation sequencing.

He Y, Yan JM, Liu YH, Han J, Li DZ. He Y, et al. J Obstet Gynaecol. 2017 Aug;37(6):809-810. doi: 10.1080/01443615.2017.1286304. Epub 2017 Mar 20. J Obstet Gynaecol. 2017. PMID: 28319678 Free article. No abstract available.

10

[Rapid preimplantation genetic diagnosis of α-thalassemia SEA deletion with blastocyst cell whole genome amplification and short fragment Gap-PCR method].

Xu H, Liu Y, Yan P, He Y, Qin J, Lou J, Zhou W. Xu H, et al. Among authors: he y. Nan Fang Yi Ke Da Xue Xue Bao. 2018 Sep 30;38(10):1250-1254. doi: 10.3969/j.issn.1673-4254.2018.10.16. Nan Fang Yi Ke Da Xue Xue Bao. 2018. PMID: 30377127 Free PMC article. Chinese.

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