Xiong Z - Search Results

1

Hutchinson-Gilford progeria syndrome accompanied by severe skeletal abnormalities in two Chinese siblings: two case reports.

Xiong Z, Lu Y, Xue J, Luo S, Xu X, Zhang L, Peng H, Li W, Chen D, Hu Z, Xia K. Xiong Z, et al. J Med Case Rep. 2013 Mar 8;7:63. doi: 10.1186/1752-1947-7-63. J Med Case Rep. 2013. PMID: 23497705 Free PMC article.

2

Mutation analysis of the NRXN1 gene in a Chinese autism cohort.

Liu Y, Hu Z, Xun G, Peng Y, Lu L, Xu X, Xiong Z, Xia L, Liu D, Li W, Zhao J, Xia K. Liu Y, et al. Among authors: xiong z. J Psychiatr Res. 2012 May;46(5):630-4. doi: 10.1016/j.jpsychires.2011.10.015. Epub 2012 Mar 9. J Psychiatr Res. 2012. PMID: 22405623

3

A novel splicing mutation in COL1A1 gene caused type I osteogenesis imperfecta in a Chinese family.

Peng H, Zhang Y, Long Z, Zhao D, Guo Z, Xue J, Xie Z, Xiong Z, Xu X, Su W, Wang B, Xia K, Hu Z. Peng H, et al. Among authors: xiong z. Gene. 2012 Jul 10;502(2):168-71. doi: 10.1016/j.gene.2012.04.023. Epub 2012 Apr 29. Gene. 2012. PMID: 22565191

4

Disruption of Contactin 4 in two subjects with autism in Chinese population.

Guo H, Xun G, Peng Y, Xiang X, Xiong Z, Zhang L, He Y, Xu X, Liu Y, Lu L, Long Z, Pan Q, Hu Z, Zhao J, Xia K. Guo H, et al. Among authors: xiong z. Gene. 2012 Sep 1;505(2):201-5. doi: 10.1016/j.gene.2012.06.051. Epub 2012 Jun 28. Gene. 2012. PMID: 22750301

5

Identification of a known GJB6 mutation in an autosomal dominant inherited Chinese family with hidrotic ectodermal dysplasia.

Mousumi T, Xiong Z, Lu L, Liu S, Xia K, Hu Z. Mousumi T, et al. Among authors: xiong z. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2013 Aug;38(8):761-5. doi: 10.3969/j.issn.1672-7347.2013.08.001. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2013. PMID: 23981984

6

Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.

Xu X, Xiong Z, Zhang L, Liu Y, Lu L, Peng Y, Guo H, Zhao J, Xia K, Hu Z. Xu X, et al. Among authors: xiong z. Mol Biol Rep. 2014 Jun;41(6):4133-40. doi: 10.1007/s11033-014-3284-5. Epub 2014 Feb 26. Mol Biol Rep. 2014. PMID: 24570023

7

Association of genetic variants of GRIN2B with autism.

Pan Y, Chen J, Guo H, Ou J, Peng Y, Liu Q, Shen Y, Shi L, Liu Y, Xiong Z, Zhu T, Luo S, Hu Z, Zhao J, Xia K. Pan Y, et al. Among authors: xiong z. Sci Rep. 2015 Feb 6;5:8296. doi: 10.1038/srep08296. Sci Rep. 2015. PMID: 25656819 Free PMC article.

8

Report of two FOP cases with 617G>A mutation in the ACVR1 gene from Chinese population.

Guo H, Peng D, Xu M, Xue J, Lu L, Xu X, Liu Y, Xiong Z, Pan Q, Hu Z, Xia K. Guo H, et al. Among authors: xiong z. Clin Dysmorphol. 2010 Oct;19(4):206-208. doi: 10.1097/MCD.0b013e32833986c8. Clin Dysmorphol. 2010. PMID: 20736820 No abstract available.

9

Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese population.

Hu Z, Xiong Z, Xu X, Li F, Lu L, Li W, Su J, Liu Y, Liu D, Xie Z, Peng Y, Kuang Y, Wu L, Zhang J, Pan Q, Tang B, Chen X, Xia K. Hu Z, et al. Among authors: xiong z. Hum Genet. 2012 Jul;131(7):1269-74. doi: 10.1007/s00439-012-1155-5. Epub 2012 Mar 11. Hum Genet. 2012. PMID: 22407025

10

Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.

Guo H, Peng Y, Hu Z, Li Y, Xun G, Ou J, Sun L, Xiong Z, Liu Y, Wang T, Chen J, Xia L, Bai T, Shen Y, Tian Q, Hu Y, Shen L, Zhao R, Zhang X, Zhang F, Zhao J, Zou X, Xia K. Guo H, et al. Among authors: xiong z. Sci Rep. 2017 Mar 10;7:44155. doi: 10.1038/srep44155. Sci Rep. 2017. PMID: 28281572 Free PMC article. Clinical Trial.

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