Geng Q - 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: geng q. 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

[The prenatal genetic diagnosis of a family with complete androgen insensitivity syndrome].

Wu WQ, Liu Y, Geng Q, Luo FW, Chen WB, Yuan H, Xie JS. Wu WQ, et al. Among authors: geng q. Zhonghua Yi Xue Za Zhi. 2016 Dec 20;96(47):3793-3796. doi: 10.3760/cma.j.issn.0376-2491.2016.47.005. Zhonghua Yi Xue Za Zhi. 2016. PMID: 28057092 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. Among authors: geng q. 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. Among authors: geng q. 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. 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: geng q. 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

[Genetic analysis and prenatal diagnosis of two Chinese families with split hand foot malformation].

Wang H, Xie J, Chen W, Geng Q, Xu X. Wang H, et al. Among authors: geng q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):280-4. doi: 10.3760/cma.j.issn.1003-9406.2014.03.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24928002 Chinese.

8

[Genetic analysis for a family with Cockayne syndrome].

Chen L, Yu S, Wu W, Geng Q, Luo F, Xie J. Chen L, et al. Among authors: geng q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):285-8. doi: 10.3760/cma.j.issn.1003-9406.2014.03.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24928003 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: geng q. 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

[Genetic and prenatal diagnosis for a Chinese family with primary carnitine deficiency].

Su Y, Liu Y, Xie J, Xu Z, Wu W, Geng Q, Luo F. Su Y, et al. Among authors: geng q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Aug;32(4):490-4. doi: 10.3760/cma.j.issn.1003-9406.2015.04.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26252091 Chinese.

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