Peng W - Search Results

1

Two novel L2HGDH mutations identified in a rare Chinese family with L-2-hydroxyglutaric aciduria.

Peng W, Ma XW, Yang X, Zhang WQ, Yan L, Wang YX, Liu X, Wang Y, Feng ZC. Peng W, et al. BMC Med Genet. 2018 Sep 14;19(1):167. doi: 10.1186/s12881-018-0675-9. BMC Med Genet. 2018. PMID: 30217188 Free PMC article.

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

Langerhans cell histiocytosis, a new clinical phenotype of x-linked lymphoproliferative disease?

Zhang X, Zhu D, Lan H, Yu L, Peng W, Mei Y, Feng Z. Zhang X, et al. Among authors: peng w. Eur J Med Genet. 2011 Mar-Apr;54(2):165-8. doi: 10.1016/j.ejmg.2010.11.006. Epub 2010 Nov 20. Eur J Med Genet. 2011. PMID: 21094704

6

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.

7

Role of bone marrow-derived mesenchymal stem cells in the prevention of hyperoxia-induced lung injury in newborn mice.

Zhang X, Wang H, Shi Y, Peng W, Zhang S, Zhang W, Xu J, Mei Y, Feng Z. Zhang X, et al. Among authors: peng w. Cell Biol Int. 2012 Jun 1;36(6):589-94. doi: 10.1042/CBI20110447. Cell Biol Int. 2012. PMID: 22339670

8

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

9

[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.

10

[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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

6,451 results

Search Page

Filters