Liu X - Search Results

1

Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy.

Wang H, Xu Y, Liu X, Wang L, Jiang W, Xiao B, Wei W, Chen Y, Ye W, Ji X. Wang H, et al. Among authors: liu x. Prenat Diagn. 2017 Apr;37(4):356-364. doi: 10.1002/pd.5019. Epub 2017 Mar 6. Prenat Diagn. 2017. PMID: 28181689

2

[Prenatal diagnosis of glycogen storage disease Ia by screening for hot spot mutations in combination with the 1176 nucleotide polymorphism linkage analysis].

Qiu WJ, Zhang YF, Pan J, Ye J, Liu XQ, Han LS, Gu XF. Qiu WJ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Feb;22(1):44-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15696478 Chinese.

3

[Genetic tests and clinical re-evaluation of 85 children with suspected spinal muscular atrophy].

Ji X, Liu XQ, Shen JW, Li XH, Tao J. Ji X, et al. Among authors: liu xq. Zhonghua Er Ke Za Zhi. 2010 Jun;48(6):425-30. Zhonghua Er Ke Za Zhi. 2010. PMID: 21055263 Chinese.

4

[Diagnostic value of neuronal nitric oxide synthase antibody for clinically suspected Becker muscular dystrophy].

Li XH, Zhao L, Wu Y, Wu J, He DK, Liu XQ. Li XH, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2011 Apr;13(4):288-91. Zhongguo Dang Dai Er Ke Za Zhi. 2011. PMID: 21507296 Free article. Chinese.

5

[Clinical application of multiplex ligation-dependent probe amplification for the detection exonic copy number alterations in the Dystrophin gene].

Long F, Sun W, Ji X, Li XH, Liu XQ, Jiang WT, Tao J. Long F, et al. Among authors: liu xq. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):699-704. doi: 10.3760/cma.j.issn.1003-9406.2011.06.023. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 22161109 Chinese.

6

[The value of high-frequency ultrasound in the diagnosis of duchenne muscular dystrophy in children].

Shi YR, Liu XQ, Dai H, Lu DY, Ni JY, Li XH. Shi YR, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2012 Jul;14(7):533-5. Zhongguo Dang Dai Er Ke Za Zhi. 2012. PMID: 22809609 Free article. Chinese.

7

[Analysis of AGG interspersion of the FMR1 gene in fragile X syndrome].

Tang L, Xiao B, Xu Y, Ji X, Jiang W, Liu X, Tao J. Tang L, et al. Among authors: liu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):11-5. doi: 10.3760/cma.j.issn.1003-9406.2015.01.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25636091 Chinese.

8

Marked yield of re-evaluating phenotype and exome/target sequencing data in 33 individuals with intellectual disabilities.

Xiao B, Qiu W, Ji X, Liu X, Huang Z, Liu H, Fan Y, Xu Y, Liu Y, Yie H, Wei W, Yan H, Gong Z, Shen L, Sun Y. Xiao B, et al. Among authors: liu y, liu x, liu h. Am J Med Genet A. 2018 Jan;176(1):107-115. doi: 10.1002/ajmg.a.38542. Epub 2017 Nov 21. Am J Med Genet A. 2018. PMID: 29159939

9

[Clinical and genetic analysis of two unrelated patients with Angelman syndrome and novel UBE3A mutations].

Xu H, Ji X, Xu Y, Liu X, Zhang J, Chen Y, Xiao B. Xu H, et al. Among authors: liu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):826-830. doi: 10.3760/cma.j.issn.1003-9406.2017.06.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188609 Chinese.

10

Novel noncontiguous duplications identified with a comprehensive mutation analysis in the DMD gene by DMD gene-targeted sequencing.

Xu Y, Wang H, Xiao B, Wei W, Liu Y, Ye H, Ying X, Chen Y, Liu X, Ji X, Sun Y. Xu Y, et al. Among authors: liu y, liu x. Gene. 2018 Mar 1;645:113-118. doi: 10.1016/j.gene.2017.12.037. Epub 2017 Dec 19. Gene. 2018. PMID: 29273555

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