Chen X - Search Results

1

Fragile X syndrome screening in Chinese children with unknown intellectual developmental disorder.

Chen X, Wang J, Xie H, Zhou W, Wu Y, Wang J, Qin J, Guo J, Gu Q, Zhang X, Ji T, Zhang Y, Xiong Z, Wang L, Wu X, Latham GJ, Jiang Y. Chen X, et al. BMC Pediatr. 2015 Jul 15;15:77. doi: 10.1186/s12887-015-0394-8. BMC Pediatr. 2015. PMID: 26174701 Free PMC article.

2

Global DNA hypomethylation is associated with NTD-affected pregnancy: A case-control study.

Chen X, Guo J, Lei Y, Zou J, Lu X, Bao Y, Wu L, Wu J, Zheng X, Shen Y, Wu BL, Zhang T. Chen X, et al. Birth Defects Res A Clin Mol Teratol. 2010 Jul;88(7):575-81. doi: 10.1002/bdra.20670. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 20641100

3

Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family.

Shen Y, Chen X, Wang L, Guo J, Shen J, An Y, Zhu H, Zhu Y, Xin R, Bao Y, Gusella JF, Zhang T, Wu BL. Shen Y, et al. Among authors: chen x. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):225-32. doi: 10.1002/ajmg.b.31147. Epub 2010 Dec 28. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21302351

4

Association study of PARD3 gene polymorphisms with neural tube defects in a Chinese Han population.

Gao Y, Chen X, Shangguan S, Bao Y, Lu X, Zou J, Guo J, Dai Y, Zhang T. Gao Y, et al. Among authors: chen x. Reprod Sci. 2012 Jul;19(7):764-71. doi: 10.1177/1933719111433886. Epub 2012 Mar 22. Reprod Sci. 2012. PMID: 22447895

5

Detection of copy number variants reveals association of cilia genes with neural tube defects.

Chen X, Shen Y, Gao Y, Zhao H, Sheng X, Zou J, Lip V, Xie H, Guo J, Shao H, Bao Y, Shen J, Niu B, Gusella JF, Wu BL, Zhang T. Chen X, et al. PLoS One. 2013;8(1):e54492. doi: 10.1371/journal.pone.0054492. Epub 2013 Jan 17. PLoS One. 2013. PMID: 23349908 Free PMC article.

6

PCMT1 gene polymorphisms, maternal folate metabolism, and neural tube defects: a case-control study in a population with relatively low folate intake.

Wang F, Wang J, Guo J, Chen X, Guan Z, Zhao H, Xie H, Liu C, Bao Y, Zou J, Niu B, Zhang T. Wang F, et al. Among authors: chen x. Genes Nutr. 2013 Nov;8(6):581-7. doi: 10.1007/s12263-013-0355-5. Epub 2013 Aug 6. Genes Nutr. 2013. PMID: 23918616 Free PMC article.

7

Recurrent 8q13.2-13.3 microdeletions associated with branchio-oto-renal syndrome are mediated by human endogenous retroviral (HERV) sequence blocks.

Chen X, Wang J, Mitchell E, Guo J, Wang L, Zhang Y, Hodge JC, Shen Y. Chen X, et al. BMC Med Genet. 2014 Aug 19;15:90. doi: 10.1186/s12881-014-0090-9. BMC Med Genet. 2014. PMID: 25135225 Free PMC article.

8

Annular pancreas in Trichorhinophalangeal syndrome type II with 8q23.3-q24.12 interstitial deletion.

Li Q, Zhang Z, Yan Y, Xiao P, Gao Z, Cheng W, Su L, Yu K, Xie H, Chen X, Jiang Q, Li L. Li Q, et al. Among authors: chen x. Mol Cytogenet. 2015 Dec 15;8:95. doi: 10.1186/s13039-015-0201-0. eCollection 2015. Mol Cytogenet. 2015. PMID: 26673557 Free PMC article.

9

[The pathogenicity of somatic mutation to common tumors and developmental malformation of the nervous system].

Liu F, Song X, Xie H, Chen XL. Liu F, et al. Among authors: chen xl. Yi Chuan. 2016 Mar;38(3):196-205. doi: 10.16288/j.yczz.15-400. Yi Chuan. 2016. PMID: 27001474 Review. Chinese.

10

A complex intragenic rearrangement of ERCC8 in Chinese siblings with Cockayne syndrome.

Xie H, Li X, Peng J, Chen Q, Gao Z, Song X, Li W, Xiao J, Li C, Zhang T, Gusella JF, Zhong J, Chen X. Xie H, et al. Among authors: chen q, chen x. Sci Rep. 2017 Mar 23;7:44271. doi: 10.1038/srep44271. Sci Rep. 2017. PMID: 28333167 Free PMC article.

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