Xu Z - Search Results

1

Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect.

Qiao F, Wang Y, Zhang C, Zhou R, Wu Y, Wang C, Meng L, Mao P, Cheng Q, Luo C, Hu P, Xu Z. Qiao F, et al. Among authors: xu z. Ultrasound Obstet Gynecol. 2021 Sep;58(3):377-387. doi: 10.1002/uog.23532. Ultrasound Obstet Gynecol. 2021. PMID: 33142350 Free article.

2

A novel competitive fluorescent multiplex STR polymorphism assay for rapid, reliable and single-tube screening of 22q11.2 copy-number aberrations.

Yang C, Shen L, Xu Z, Wu X, Mo X, Zhang J, Wang D, Wang Y, Peng Y, Cao L, Jiang Y, Gu H, Chen S, Bian X, Liu J, Qiao D, Yi L. Yang C, et al. Among authors: xu z. Electrophoresis. 2009 Feb;30(3):465-71. doi: 10.1002/elps.200800321. Electrophoresis. 2009. PMID: 19145597

3

[Prenatal genetic study of fetuses with congenital heart diseases].

Xu ZF, Cao L, Ji XQ, Yang C, Zhang JJ, Xu QJ, Zha W, Yang YQ, Lin YS, Chen CH, Liu A, Li L, Lin Y, Yi L. Xu ZF, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Apr;26(2):128-33. doi: 10.3760/cma.j.issn.1003-9406.2009.02.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19350500 Chinese.

4

[Detection of cryptic copy number variations in a fetus with congenital heart disease by array-based comparative genomic hybridization].

HU P, WANG Y, JI XQ, LIN Y, Li L, ZHOU XY, CHEN J, MA DY, CAO L, Xu Z. HU P, et al. Among authors: xu z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Apr;28(2):133-6. doi: 10.3760/cma.j.issn.1003-9406.2011.02.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21462121 Chinese.

5

22q11.2 microduplication in a family with recurrent fetal congenital heart disease.

Hu P, Ji X, Yang C, Zhang J, Lin Y, Cheng J, Ma D, Cao L, Yi L, Xu Z. Hu P, et al. Among authors: xu z. Eur J Med Genet. 2011 Jul-Aug;54(4):e433-6. doi: 10.1016/j.ejmg.2011.03.009. Epub 2011 Apr 5. Eur J Med Genet. 2011. PMID: 21473936

6

[Application of multiplex ligation-dependent probe amplification for rapid detection of aneuploidies in prenatal diagnosis].

Ma DY, Hu P, Zhang JJ, Yi L, Ji XQ, Yang C, Cheng J, Li L, Lin Y, Xu ZF. Ma DY, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Oct;28(5):543-7. doi: 10.3760/cma.j.issn.1003-9406.2011.05.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21983731 Chinese.

7

[ASS1 mutation leading to citrullinemia I in a Chinese Han family].

Hu P, Zhou XY, Ma DY, Sun Y, Zhang XJ, Han SP, Yu ZB, Jiang T, Chen YL, Xu Z. Hu P, et al. Among authors: xu z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):630-3. doi: 10.3760/cma.j.issn.1003-9406.2011.06.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 22161093 Chinese.

8

[Detection of 9p partial trisomy using array-based comparative genomic hybridization].

Zhou XY, Hu P, Yang YQ, Li L, Wang Y, Yu ZB, Han SP, Guo XR, Xu ZF. Zhou XY, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Feb;29(1):52-5. doi: 10.3760/cma.j.issn.1003-9406.2012.01.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22311492 Chinese.

9

[Cytogenetic analysis of a complex chromosomal imbalance 14q+ in a fetus featuring multiple congenital defects].

Li L, Zhou XY, Ji XQ, Yang YQ, Cao L, Zhou J, Liu A, Cheng J, Liu Y, Hu P, Xu ZF. Li L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Apr;29(2):214-7. doi: 10.3760/cma.j.issn.1003-9406.2012.02.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22487837 Chinese.

10

[Array-based comparative genomic hybridization detection of copy number variations in a fetus with hypoplastic left-heart syndrome].

Wang Y, Ma DY, Yang YQ, Zhou J, Zhou XY, Ji XQ, Chen J, Cao L, Hu P, Xu ZF. Wang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):439-42. doi: 10.3760/cma.j.issn.1003-9406.2012.04.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875502 Chinese.

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