Cheng H - Search Results

1

Importance of a semen analysis report for determining the relationship between SCSA sperm DNA fragmentation index and assisted reproductive technology pregnancy rate.

Cheng H, Han M, Ding J, Wang F, Wang G, Shen L, Wang J, Zheng B, Meng Q, Wang W, Yang S, Li H. Cheng H, et al. Reprod Biol. 2020 Dec;20(4):460-464. doi: 10.1016/j.repbio.2019.09.002. Epub 2020 Aug 12. Reprod Biol. 2020. PMID: 32798137

2

A novel mutation (C1425Y) in the FBN2 gene in a father and son with congenital contractural arachnodactyly.

Chen Y, Lei YP, Zheng HX, Wang W, Cheng HB, Zhang J, Wang HY, Jin L, Li H. Chen Y, et al. Among authors: cheng hb. Genet Test Mol Biomarkers. 2009 Jun;13(3):295-300. doi: 10.1089/gtmb.2008.0132. Genet Test Mol Biomarkers. 2009. PMID: 19473076

3

A novel mutation of GATA4 in a familial atrial septal defect.

Chen Y, Mao J, Sun Y, Zhang Q, Cheng HB, Yan WH, Choy KW, Li H. Chen Y, et al. Among authors: cheng hb. Clin Chim Acta. 2010 Nov 11;411(21-22):1741-5. doi: 10.1016/j.cca.2010.07.021. Epub 2010 Jul 24. Clin Chim Acta. 2010. PMID: 20659440

4

[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: cheng 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.

5

[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: cheng hb. Zhonghua Er Ke Za Zhi. 2011 Apr;49(4):316-9. Zhonghua Er Ke Za Zhi. 2011. PMID: 21624212 Chinese.

6

[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: cheng 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.

7

[Analysis of GJB2 gene and mitochondrial DNA A1555G mutations in 16 families with non-syndromic hearing loss].

Wang W, Cheng HB, Yang N, Shi YC, Liu JZ, Li Q, Yang SM, Shen LY, Liu MJ, Chen Y, Li H. Wang W, et al. Among authors: cheng hb. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):388-92. doi: 10.3760/cma.j.issn.1003-9406.2012.04.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875492 Chinese.

8

[A pedigree with blepharophimosis-ptosis-epicanthus inversus syndrome].

Cheng H, Yang N, Liu J, Song L, Wang T, Lin LQ, Xu Q, Yang S, Shen L, Song D, Wang T, Wang W, Shi Y, Li H. Cheng H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Jun;30(3):382. doi: 10.3760/cma.j.issn.1003-9406.2013.03.032. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23744336 Chinese. No abstract available.

9

[Non-syndromic autosomal dominant type deafness: report of a family with 26 cases].

Liu JZ, Cheng HB, Yang N, Lin LQ, Xu QY, Gu X, Shi YC, Yang SM, Shen LY, Song D, Wang T, Wang W, Li Q, Li H. Liu JZ, et al. Among authors: cheng hb. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Aug;30(4):501. doi: 10.3760/cma.j.issn.1003-9406.2013.04.025. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23926024 Chinese. No abstract available.

10

[The value of histopathologic examination of testis tissue from testicular sperm aspiration].

Yang SM, Chen B, Shi YC, Wen DG, Li H, Wang W, Cheng HB. Yang SM, et al. Among authors: cheng hb. Zhonghua Nan Ke Xue. 2013 Oct;19(10):899-901. Zhonghua Nan Ke Xue. 2013. PMID: 24218943 Chinese.

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