Xu Z - Search Results

1

The Cation Channel TMEM63B Is an Osmosensor Required for Hearing.

Du H, Ye C, Wu D, Zang YY, Zhang L, Chen C, He XY, Yang JJ, Hu P, Xu Z, Wan G, Shi YS. Du H, et al. Among authors: xu z. Cell Rep. 2020 May 5;31(5):107596. doi: 10.1016/j.celrep.2020.107596. Cell Rep. 2020. PMID: 32375046 Free article.

2

[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.

3

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

4

[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.

5

[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.

6

[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.

7

[Prenatal diagnosis of two fetuses with de novo small supernumerary markers by single nucleotide polymorphism array based comparative genomic hybridization].

Ji XQ, Li L, Lin Y, Ma DY, Liu A, Zhang JJ, Cheng J, Zhou J, Hu P, Xu ZF. Ji XQ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Oct;29(5):510-4. doi: 10.3760/cma.j.issn.1003-9406.2012.05.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23042383 Chinese.

8

[Molecular diagnosis of OTC gene mutation in a Chinese family with ornithine transcarbamylase deficiency].

Meng LL, Jiang T, Qin L, Ma DY, Chen YL, Han SP, Yu ZB, Guo XR, Hu P, Xu ZF. Meng LL, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Apr;30(2):195-8. doi: 10.3760/cma.j.issn.1003-9406.2013.04.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23568734 Chinese.

9

1q25.2-q31.3 Deletion in a female with mental retardation, clinodactyly, minor facial anomalies but no growth retardation.

Hu P, Wang Y, Meng LL, Qin L, Ma DY, Yi L, Xu ZF. Hu P, et al. Mol Cytogenet. 2013 Aug 6;6(1):30. doi: 10.1186/1755-8166-6-30. Mol Cytogenet. 2013. PMID: 23915434 Free PMC article.

10

[Prenatal diagnosis of 22q11.2 microdeletion by multiplex ligation-dependent probe amplification].

Luo CY, Ma DY, Zhang JJ, Hu P, Cao L, Ji XQ, Zhou J, Liu A, Wu Y, Cheng J, Lin Y, Xu ZF. Luo CY, et al. Zhonghua Fu Chan Ke Za Zhi. 2013 Nov;48(11):824-7. Zhonghua Fu Chan Ke Za Zhi. 2013. PMID: 24444558 Chinese.

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