Li HB - Search Results

1

A patient with five chromosomal rearrangements and a 2q31.1 microdeletion.

Wang T, Mao J, Liu MJ, Choy KW, Li HB, Cram DS, Li H, Chen Y. Wang T, et al. Among authors: li h, li hb. Clin Chim Acta. 2014 Mar 20;430:129-33. doi: 10.1016/j.cca.2014.01.002. Epub 2014 Jan 9. Clin Chim Acta. 2014. PMID: 24412318

2

[22q11 microdeletion test in patients with congenital heart defects by quantitative fluorescent PCR].

Chen Y, Mao J, Kwok KY, Kan HJ, Cheng HB, Li HB, Liu MJ, Sun Y, Yan WH, Li H, Choy KW. Chen Y, et al. Among authors: li h, li hb. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Oct;27(5):571-5. doi: 10.3760/cma.j.issn.1003-9406.2010.05.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20931540 Chinese.

3

[Clinical detection of 22q11 microdeletion in the patients with congenital heart disease by multiplex ligation dependent probe amplification].

Chen Y, Kan HJ, Mao J, Ding J, Meng QX, Li HB, Cheng HB, Liu MJ, Sun Y, Yan WH, Li H. Chen Y, et al. Among authors: li h, li hb. Zhonghua Er Ke Za Zhi. 2011 Apr;49(4):316-9. Zhonghua Er Ke Za Zhi. 2011. PMID: 21624212 Chinese.

4

[Genetic screening of mutation hot-spots for nonsyndromic hearing loss in southern Jiangsu province with SNaPshot].

Li H, Li HB, Mao J, Liu MJ, Cheng HB, Li SL, Chen Y. Li H, et al. Among authors: li sl, li hb. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):383-6. doi: 10.3760/cma.j.issn.1003-9406.2011.04.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21811975 Chinese.

5

[A literature review of epidemiological studies on mutation hot spots of Chinese population with non-syndromic hearing loss].

Li H, Li Q, Li H, Chen Y. Li H, et al. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Jul;26(13):589-94. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 23002642 Review. Chinese.

6

[Genetic analysis of a family with super-male syndrome].

Zhang J, Li H, Jiang S, Chen Y, Zhang Y. Zhang J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Apr;31(2):210-3. doi: 10.3760/cma.j.issn.1003-9406.2014.02.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24711034 Chinese.

7

[A microdeletion of chromosome 9q34.11 may cause suspected cerebral palsy].

Li H, Chen Y, Li Q, Liu M, Mao J, Song D, Li H. Li H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):725-9. doi: 10.3760/cma.j.issn.1003-9406.2014.06.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449075 Chinese.

8

Morphological characteristics and initial genetic study of multiple morphological anomalies of the flagella in China.

Yang SM, Li HB, Wang JX, Shi YC, Cheng HB, Wang W, Li H, Hou JQ, Wen DG. Yang SM, et al. Among authors: li h, li hb. Asian J Androl. 2015 May-Jun;17(3):513-5. doi: 10.4103/1008-682X.146100. Asian J Androl. 2015. PMID: 25652624 Free PMC article. No abstract available.

9

[Systematic genetic analysis for a case with duplication 9p].

Zhang J, Li H, Jiang S, Li H, Zhang Y. Zhang J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Apr;32(2):237-9. doi: 10.3760/cma.j.issn.1003-9406.2015.02.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25863095 Chinese.

10

SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes.

Li H, Wang B, Liu D, Wang T, Li Q, Wang W, Li H. Li H, et al. Genomics. 2015 Aug;106(2):83-7. doi: 10.1016/j.ygeno.2015.05.004. Epub 2015 May 22. Genomics. 2015. PMID: 26004784 Free article.

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