Wang CZ - Search Results

1

[Genetic analysis of a supernumerary derivative chromosome 15].

Wang F, Yang Y, Wang CZ, He XI. Wang F, et al. Among authors: wang cz. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Feb;29(1):77-81. doi: 10.3760/cma.j.issn.1003-9406.2012.01.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22311498 Chinese.

2

[Detection of the genetic abnormalities in patients with mental retardation using multiplex ligation-dependent probe amplification assay].

Zhu L, Wang C, Yang X, Wang Y, Liu X, He X. Zhu L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Dec;26(6):644-7. doi: 10.3760/cma.j.issn.1003-9406.2009.06.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19953486 Chinese.

3

Novel chromosomal translocation t(11;9)(p15;p23) involving deletion and duplication of 9p in a girl associated with autism and mental retardation.

Yang Y, Wang C, Wang F, Zhu L, Liu H, He X. Yang Y, et al. Gene. 2012 Jul 10;502(2):154-8. doi: 10.1016/j.gene.2012.04.036. Epub 2012 Apr 24. Gene. 2012. PMID: 22555022

4

[Analysis of clinical features, metabolic profiling and gene mutations of patients with ornithine transcarbamylase deficiency].

Wang Y, Liu X, Wu H, Liu H, Wang C, He X. Wang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Apr;31(2):148-51. doi: 10.3760/cma.j.issn.1003-9406.2014.02.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24711021 Chinese.

5

[Chromosome analysis in 92 children with congenital mental retardation].

Wang F, Yang Y, Yang X, Wang CZ, He XY. Wang F, et al. Among authors: wang cz. Zhongguo Dang Dai Er Ke Za Zhi. 2011 Aug;13(8):651-3. Zhongguo Dang Dai Er Ke Za Zhi. 2011. PMID: 21849116 Free article. Chinese.

6

[Value of methylation-specific mutiplex ligation-dependent probe in the diagnosis of Prader-Willi syndrome].

Zhan SN, Wang CZ, Yang Y, Wang Y, Wu HL, Li H, He XY. Zhan SN, et al. Among authors: wang y, wang cz. Zhongguo Dang Dai Er Ke Za Zhi. 2012 Jun;14(6):445-8. Zhongguo Dang Dai Er Ke Za Zhi. 2012. PMID: 22738453 Free article. Chinese.

7

Whole dystrophin gene analysis by next-generation sequencing: a comprehensive genetic diagnosis of Duchenne and Becker muscular dystrophy.

Wang Y, Yang Y, Liu J, Chen XC, Liu X, Wang CZ, He XY. Wang Y, et al. Among authors: wang cz. Mol Genet Genomics. 2014 Oct;289(5):1013-21. doi: 10.1007/s00438-014-0847-z. Epub 2014 Apr 27. Mol Genet Genomics. 2014. PMID: 24770780

8

Four novel GALC gene mutations in two Chinese patients with Krabbe disease.

Yang Y, Ren X, Xu Q, Wang C, Liu H, He X. Yang Y, et al. Gene. 2013 May 1;519(2):381-4. doi: 10.1016/j.gene.2013.02.010. Epub 2013 Feb 24. Gene. 2013. PMID: 23462331

9

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. Respir Care. 2011 Jul;56(7):1009-15. doi: 10.4187/respcare.01032. Epub 2011 Feb 9. Respir Care. 2011. PMID: 21310116 Free article.

10

Reference intervals for serum thyroid hormones in preterm hospitalized infants.

Zhu L, Zhang X, He X, Yang X, Wang Y, Wang C, Feng Z. Zhu L, et al. J Pediatr Endocrinol Metab. 2013;26(5-6):463-7. doi: 10.1515/jpem-2012-0277. J Pediatr Endocrinol Metab. 2013. PMID: 23412903

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