Yang Y - Search Results

1

[Mutation analysis and prenatal diagnosis of families affected with Duchenne and Becker muscular dystrophy].

Wang WJ, Zhu HY, Zhu RF, Yang Y, Zhu XY, Duan HL, Zhang Y, Wu X. Wang WJ, et al. Among authors: yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Feb;30(1):45-8. doi: 10.3760/cma.j.issn.1003-9406.2013.01.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23450478 Chinese.

2

[Molecular genetics study of ED1 gene for two X-linked hypohidrotic ectodermal dysplasia families].

Zhu HI, Wang WJ, Zhu RF, Zhu XY, Yang Y, Wu X. Zhu HI, et al. Among authors: yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Aug;30(4):399-402. doi: 10.3760/cma.j.issn.1003-9406.2013.04.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23926003 Chinese.

3

[Application of different technologies for distinguishing true and pseudo mosaicisms during prenatal diagnosis].

Zhu R, Zhu X, Yang Y, Duan H, Zhang Y, Wu X, Wang W, Li J. Zhu R, et al. Among authors: yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Oct;31(5):636-40. doi: 10.3760/cma.j.issn.1003-9406.2014.01.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25297599 Chinese.

4

[Application of chromosome microarray analysis for prenatal diagnosis of a fetus with partial duplication of 1p and uniparental disomy of chromosome 6].

Zhu R, Zhu X, Wang Y, Li J, Ru T, Yang Y. Zhu R, et al. Among authors: yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Dec;32(6):819-22. doi: 10.3760/cma.j.issn.1003-9406.2015.06.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26663056 Chinese.

5

[Chromosome microarray analysis of four fetuses with abnormal karyotypes].

Zhu R, Zhu X, Yang Y, Wu X, Zhang Y, Shi Y, He L, Li J. Zhu R, et al. Among authors: yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):812-815. doi: 10.3760/cma.j.issn.1003-9406.2017.06.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188606 Chinese.

6

[Mutation analysis for a methylmalonic acidemia pedigree without proband by high-throughput sequencing].

Cao P, Zhu X, Yang Y, Zhu Y, Li J. Cao P, et al. Among authors: yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Jun 10;35(3):397-399. doi: 10.3760/cma.j.issn.1003-9406.2018.03.020. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29896740 Chinese.

7

[Application of chromosomal microarray analysis in prenatal diagnosis of fetuses with increased nuchal translucency].

Ni M, Li J, Zhu X, Zhu Y, Gu L, Wu X, Yang Y. Ni M, et al. Among authors: yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Oct 10;36(10):970-974. doi: 10.3760/cma.j.issn.1003-9406.2019.10.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31598938 Chinese.

8

[Mutational analysis in a family with X-linked spondyloepiphyseal dysplasia tarda].

Zhu HY, Li J, Zhu RF, Wu X, Duan HL, Yang Y, Zhang Y, Hu Y. Zhu HY, et al. Among authors: yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Aug;25(4):421-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18683141 Chinese.

9

[Rapid genetic prenatal diagnosis for achondroplasia].

Zhu HY, Yang Y, Li J, Ru T, Hu YL. Zhu HY, et al. Among authors: yang y. Zhonghua Fu Chan Ke Za Zhi. 2008 Nov;43(11):810-3. Zhonghua Fu Chan Ke Za Zhi. 2008. PMID: 19087561 Chinese.

10

[Application of multiplex quantitative fluorescent PCR with non-polymorphic loci in prenatal diagnosis].

Zhu XY, Hu YL, Wang YP, Zhu HY, Li J, Zhu RF, Zhang Y, Wu X, Yang Y. Zhu XY, et al. Among authors: yang y. Zhonghua Fu Chan Ke Za Zhi. 2008 Nov;43(11):818-23. Zhonghua Fu Chan Ke Za Zhi. 2008. PMID: 19087563 Chinese.

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