Xu Z - Search Results

1

[Genetic analysis and prenatal diagnosis for ten families affected with tuberous sclerosis complex].

Pan Y, Wu W, Luo C, Xie J, Xu Z, Geng Q, Hao Y. Pan Y, et al. Among authors: xu z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Feb 10;35(1):18-22. doi: 10.3760/cma.j.issn.1003-9406.2018.01.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29419853 Chinese.

2

[Molecular and prenatal diagnosis for a Chinese pregnant woman with a novel mutation of β thalassemia].

Hao Y, Xu ZY, Jin Q, Wu WQ, Cai J, Luo CQ, Xie JS. Hao Y, et al. Zhonghua Xue Ye Xue Za Zhi. 2011 Apr;32(4):245-8. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 21569707 Chinese.

3

[Clinical significance of large-scale screening of A1555G mutation of mitochondria DNA for neonates].

Cai J, Luo CQ, Xie JS, Wu WQ, Geng Q, Xu ZY, Hao Y, Xu XX. Cai J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):414-6. doi: 10.3760/cma.j.issn.1003-9406.2011.04.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21811982 Chinese.

4

[Genetic analysis and prenatal diagnosis for a family with megalencephalic leukoencephalopathy and subcortical cysts].

Wu WQ, Xie JS, Han CX, Xu ZY, Geng Q, Yuan H. Wu WQ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):616-9. doi: 10.3760/cma.j.issn.1003-9406.2011.06.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 22161090 Chinese.

5

[Application of array-CGH and MLPA for detection of 4 cryptic unbalanced translocations].

Geng Q, Wu W, Luo F, Xu Z, Chen W, Li F, Xie J. Geng Q, et al. Among authors: xu z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Jun;30(3):288-92. doi: 10.3760/cma.j.issn.1003-9406.2013.03.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23744316 Chinese.

6

[A novel mutation of cartilage oligomeric matrix protein gene underlies multiple epiphyseal dysplasia].

Wang H, Xie J, Wu W, Xu Z, Luo F, Geng Q. Wang H, et al. Among authors: xu z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Jun;30(3):322-5. doi: 10.3760/cma.j.issn.1003-9406.2013.03.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23744324 Chinese.

7

A novel splicing mutation in the SEDL gene causes spondyloepiphyseal dysplasia tarda in a large Chinese pedigree.

Wang H, Wu W, Xu Z, Xie J. Wang H, et al. Among authors: xu z. Clin Chim Acta. 2013 Oct 21;425:30-3. doi: 10.1016/j.cca.2013.07.002. Epub 2013 Jul 19. Clin Chim Acta. 2013. PMID: 23876379

8

[Cytogenetic and molecular analysis of idic(Yp) in 1 infertile man and 1 prenatal fetus].

Geng Q, Luo FW, Wu WQ, Xu ZY, Wang L, Wang Q, Xie JS. Geng Q, et al. Zhonghua Nan Ke Xue. 2013 Jul;19(7):642-6. Zhonghua Nan Ke Xue. 2013. PMID: 23926684 Chinese.

9

[A novel mutation in GCH1 gene causes dopa-responsive dystonia].

Wu W, Han C, Hao Y, Xie J, Xu Z, Geng Q. Wu W, et al. Among authors: xu z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Aug;31(4):420-3. doi: 10.3760/cma.j.issn.1003-9406.2014.04.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25119902 Chinese.

10

Multiplex ligation-dependent probe amplification and array comparative genomic hybridization analyses for prenatal diagnosis of cytogenomic abnormalities.

Xu Z, Geng Q, Luo F, Xu F, Li P, Xie J. Xu Z, et al. Among authors: xu f. Mol Cytogenet. 2014 Dec 9;7(1):84. doi: 10.1186/s13039-014-0084-5. eCollection 2014. Mol Cytogenet. 2014. PMID: 25530804 Free PMC article.

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