Zhu XY - Search Results

1

Mutation analysis and prenatal diagnosis of EXT1 gene mutations in Chinese patients with multiple osteochondromas.

Zhu HY, Hu YL, Yang Y, Wu X, Zhu RF, Zhu XY, Duan HL, Zhang Y, Zhou JY. Zhu HY, et al. Among authors: zhu rf, zhu xy. Chin Med J (Engl). 2011 Oct;124(19):3054-7. Chin Med J (Engl). 2011. PMID: 22040554

2

[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: zhu rf, zhu hy. Zhonghua Fu Chan Ke Za Zhi. 2008 Nov;43(11):818-23. Zhonghua Fu Chan Ke Za Zhi. 2008. PMID: 19087563 Chinese.

3

[Multiplex quantitative PCR detection for female carrier in an X-linked ichthyosis family].

Zhu HY, Li HB, Wu LQ, Zhu XY, Li J, Yang Y, Zhu RF, Wu X, Duan HL, Zhang Y, Hu YL. Zhu HY, et al. Among authors: zhu rf, zhu xy. Zhonghua Yi Xue Za Zhi. 2008 Dec 16;88(46):3246-9. Zhonghua Yi Xue Za Zhi. 2008. PMID: 19159546 Clinical Trial. Chinese.

4

Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery.

Hu Y, Zhu X, Yang Y, Mo X, Sheng M, Yao J, Wang D. Hu Y, et al. Cardiol Young. 2009 Apr;19(2):179-84. doi: 10.1017/S1047951109003667. Epub 2009 Feb 19. Cardiol Young. 2009. PMID: 19224675

5

[Mutation analysis and prenatal diagnosis of sporadic DMD/BMD families].

Zhu HY, Li J, Yang Y, Wu X, Zhu XY, Zhu RF, Zhang Y, Duan HL, Hu YL. Zhu HY, et al. Among authors: zhu rf, zhu xy. Zhonghua Yi Xue Za Zhi. 2009 Jul 7;89(25):1753-6. Zhonghua Yi Xue Za Zhi. 2009. PMID: 19862979 Chinese.

6

Comparative study of three PCR-based copy number variant approaches, CFMSA, M-PCR, and MLPA, in 22q11.2 deletion syndrome.

Yang C, Zhu X, Yi L, Shi Z, Wang H, Hu Y, Wang Y. Yang C, et al. Genet Test Mol Biomarkers. 2009 Dec;13(6):803-8. doi: 10.1089/gtmb.2009.0058. Genet Test Mol Biomarkers. 2009. PMID: 20001582

7

[Diagnosis of 22q11 deletion and duplication in congenital heart disease by multiplex ligation dependent probe amplification].

Yang YH, Hu YL, Zhu XY, Mo XM, Wang DJ, Yao JC, Sheng M, Zhu HY, Li J, Ru T, Wang ZQ. Yang YH, et al. Among authors: zhu xy, zhu hy. Zhongguo Dang Dai Er Ke Za Zhi. 2009 Nov;11(11):892-6. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 20113655 Free article. Chinese.

8

[Molecular genetic study of MECP2 gene for a patient with typical Rett syndrome].

Zhu HY, Hu YL, Zhu RF, Yang Y, Zhu XY, Wang WJ, Duan HL. Zhu HY, et al. Among authors: zhu rf, zhu xy. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):625-9. doi: 10.3760/cma.j.issn.1003-9406.2011.06.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 22161092 Chinese.

9

A boy with partial trisomy of chromosome 3q24-q28 from paternal balanced insertion and multiple congenital anomalies.

Zhu H, Hu Y, Zhu R, Yang Y, Zhu X, Wang W. Zhu H, et al. Am J Med Genet A. 2013 Feb;161A(2):327-30. doi: 10.1002/ajmg.a.35637. Epub 2013 Jan 15. Am J Med Genet A. 2013. PMID: 23322595

10

[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: zhu rf, zhu hy, zhu xy. 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.

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

1,324 results

Search Page

Filters