Geng Q - Search Results

1

Identification of two missense mutations of ERCC6 in three Chinese sisters with Cockayne syndrome by whole exome sequencing.

Yu S, Chen L, Ye L, Fei L, Tang W, Tian Y, Geng Q, Yi X, Xie J. Yu S, et al. Among authors: geng q. PLoS One. 2014 Dec 2;9(12):e113914. doi: 10.1371/journal.pone.0113914. eCollection 2014. PLoS One. 2014. PMID: 25463447 Free PMC article.

2

[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.

3

[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.

4

[Mutation analysis of the androgen receptor gene in a complete androgen insensitivity syndrome family].

Wu W, Luo F, Geng Q, Hao Y, Chen W, Cai J, Xie J. Wu W, et al. Among authors: geng q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Dec;26(6):606-9. doi: 10.3760/cma.j.issn.1003-9406.2009.06.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19953479 Chinese.

5

[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.

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

[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.

8

Prenatal Diagnosis of Twin Fetuses with a Novel AR Gene Mutation in a Chinese Family of Complete Androgen Insensitivity Syndrome.

Wu W, Geng Q, Liu Y, Xu Z, Li P, Xie J. Wu W, et al. Among authors: geng q. Fetal Pediatr Pathol. 2017 Dec;36(6):432-436. doi: 10.1080/15513815.2017.1332120. Epub 2017 Dec 5. Fetal Pediatr Pathol. 2017. PMID: 29206494

9

[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.

10

[46,XY DSD induced by a novel mutation c.458T>C (p.Leu153Pro) of the LHCGR gene: A case report and review of the literature].

Xu ZY, Zhang JX, Liu Y, Geng Q, Xie JS, Li XJ. Xu ZY, et al. Among authors: geng q. Zhonghua Nan Ke Xue. 2020 Dec;26(12):1105-1111. Zhonghua Nan Ke Xue. 2020. PMID: 34898086 Review. Chinese.

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