Peng W - Search Results

1

[Association between IL-6 C-572G and susceptibility to spontaneous preterm birth].

Yang X, Peng W, Zhu LN, Zhang XA, Wang Y. Yang X, et al. Among authors: peng w. Zhongguo Dang Dai Er Ke Za Zhi. 2017 Jul;19(7):806-811. doi: 10.7499/j.issn.1008-8830.2017.07.015. Zhongguo Dang Dai Er Ke Za Zhi. 2017. PMID: 28697836 Free PMC article. Chinese.

2

[A case report of 13q partial trisomy syndrome].

Peng W, Yang X, Zhu LN, Ma N, Liu X, Wang W. Peng W, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2009 Aug;11(8):700-1. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 19695208 Free article. Chinese. No abstract available.

3

[RABL2B gene mutation in a girl with mental retardation and hyperactivity].

Zhu LN, Liu X, Wang CZ, Wang Y, Yang X, Peng W, Wang W, Ma N. Zhu LN, et al. Among authors: peng w. Zhongguo Dang Dai Er Ke Za Zhi. 2009 Sep;11(9):780-1. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 19755037 Free article. Chinese. No abstract available.

4

[Congenital malformations in children: cytogenetic analysis of 100 cases].

Yang X, Zhu LN, Peng W. Yang X, et al. Among authors: peng w. Zhongguo Dang Dai Er Ke Za Zhi. 2010 Jan;12(1):62-3. Zhongguo Dang Dai Er Ke Za Zhi. 2010. PMID: 20113638 Free article. Chinese. No abstract available.

5

MicroRNA expression profile in hyperoxia-exposed newborn mice during the development of bronchopulmonary dysplasia.

Zhang X, Peng W, Zhang S, Wang C, He X, Zhang Z, Zhu L, Wang Y, Feng Z. Zhang X, et al. Among authors: peng w. Respir Care. 2011 Jul;56(7):1009-15. doi: 10.4187/respcare.01032. Epub 2011 Feb 9. Respir Care. 2011. PMID: 21310116 Free article.

6

A novel silent deletion, an insertion mutation and a nonsense mutation in the TCOF1 gene found in two Chinese cases of Treacher Collins syndrome.

Wang Y, Yin XJ, Han T, Peng W, Wu HL, Liu X, Feng ZC. Wang Y, et al. Among authors: peng w. Mol Genet Genomics. 2014 Dec;289(6):1237-40. doi: 10.1007/s00438-014-0883-8. Epub 2014 Jul 4. Mol Genet Genomics. 2014. PMID: 24994558

7

[A case-control study on association between OAS1 polymorphism and susceptibility to spontaneous preterm birth and preterm premature rupture of membranes].

Yang X, Zhang XA, Wu ZH, Peng W, Zhu LN, Wang Y. Yang X, et al. Among authors: peng w. Zhongguo Dang Dai Er Ke Za Zhi. 2015 Sep;17(9):898-902. Zhongguo Dang Dai Er Ke Za Zhi. 2015. PMID: 26412166 Free article. Chinese.

8

[Detection of subtelomeric copy number variations in children with intellectual disability].

Zhu LN, Wang Y, Peng W, Ma XW, Yang X, Liu X, Feng ZC. Zhu LN, et al. Among authors: peng w. Zhongguo Dang Dai Er Ke Za Zhi. 2015 Dec;17(12):1273-6. Zhongguo Dang Dai Er Ke Za Zhi. 2015. PMID: 26695663 Free article. Chinese.

9

The prospective evaluation of viral loads in patients with severe fever with thrombocytopenia syndrome.

Yang ZD, Hu JG, Lu QB, Guo CT, Cui N, Peng W, Wang LY, Qin SL, Wang HY, Zhang PH, Zhang XA, Liu W, Cao WC. Yang ZD, et al. Among authors: peng w. J Clin Virol. 2016 May;78:123-8. doi: 10.1016/j.jcv.2016.03.017. Epub 2016 Mar 17. J Clin Virol. 2016. PMID: 27062673

10

The platelet derived growth factor-B polymorphism is associated with risk of severe fever with thrombocytopenia syndrome in Chinese individuals.

Zhang XA, Guo CT, Lu QB, Hu JG, Cui N, Yang ZD, Peng W, Liu R, Hu CY, Qin SL, Wang XJ, Ding SJ, Huang DD, Liu W, Cao WC. Zhang XA, et al. Among authors: peng w. Oncotarget. 2016 May 31;7(22):33340-9. doi: 10.18632/oncotarget.9043. Oncotarget. 2016. PMID: 27147565 Free PMC article.

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