Lu X - Search Results

1

Two patients with small chromosome 22q11.21 alterations and central nervous system abnormalities.

Guy C, Wang X, Lu X, Lu J, Li S. Guy C, et al. Among authors: lu j, lu x. Mol Cytogenet. 2015 Dec 30;8:102. doi: 10.1186/s13039-015-0200-1. eCollection 2015. Mol Cytogenet. 2015. PMID: 26719767 Free PMC article.

2

16p13.3 duplication associated with non-syndromic pierre robin sequence with incomplete penetrance.

Sun M, Zhang H, Li G, Wang X, Lu X, Sternenberger A, Guy C, Li W, Lee J, Zheng L, Li S. Sun M, et al. Among authors: lu x. Mol Cytogenet. 2014 Nov 25;7(1):76. doi: 10.1186/s13039-014-0076-5. eCollection 2014. Mol Cytogenet. 2014. PMID: 25493098 Free PMC article.

3

Two rare cases of acute myeloid leukemia with t(8;16)(p11.2;p13.3) and 1q duplication: case presentation and literature review.

Liu M, Ren Y, Wang X, Lu X, Li M, Kim YM, Li S, Zhang L. Liu M, et al. Among authors: lu x. Mol Cytogenet. 2020 Aug 25;13:37. doi: 10.1186/s13039-020-00507-0. eCollection 2020. Mol Cytogenet. 2020. PMID: 32863883 Free PMC article.

4

Molecular cytogenetic characterization of partial trisomy of the long arm of chromosome 11 in a patient with multiple congenital anomalies.

Walker A, Wang X, Kim YM, Lu X, Taylor A, Demarzo D, Li S, Pang H. Walker A, et al. Among authors: lu x. Mol Cytogenet. 2022 Apr 19;15(1):17. doi: 10.1186/s13039-022-00595-0. Mol Cytogenet. 2022. PMID: 35440058 Free PMC article. Review.

5

A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0).

Lee J, Lu X, Shin ES, Kern WF, Mulvihill JJ, Li S. Lee J, et al. Among authors: lu x. Cancer Genet Cytogenet. 2008 Feb;181(1):36-9. doi: 10.1016/j.cancergencyto.2007.10.012. Cancer Genet Cytogenet. 2008. PMID: 18262051

6

Acquired genomic copy number changes in CML patients with the Philadelphia chromosome (Ph+).

Lu X, Wang X, Kim Y, Zhang R, Li S, Lee JY. Lu X, et al. Cancer Genet. 2012 Oct;205(10):513-8. doi: 10.1016/j.cancergen.2012.08.004. Epub 2012 Oct 2. Cancer Genet. 2012. PMID: 23036696

7

Clinical report: variable phenotypic expression in a large sibling cohort with a deletion of 4p16.1.

Guy C, Wang X, Lu X, Lu J, Li S. Guy C, et al. Among authors: lu j, lu x. Clin Case Rep. 2016 Aug 18;4(10):913-918. doi: 10.1002/ccr3.638. eCollection 2016 Oct. Clin Case Rep. 2016. PMID: 27761238 Free PMC article.

8

Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization.

Sun M, Zhang H, Li G, Guy CJ, Wang X, Lu X, Gong F, Lee J, Hassed S, Li S. Sun M, et al. Among authors: lu x. Sci Rep. 2017 Sep 4;7(1):10395. doi: 10.1038/s41598-017-10466-z. Sci Rep. 2017. PMID: 28871159 Free PMC article.

9

Difference of genomic copy numbers alterations between hairy cell leukemia-variant and classical hairy cell leukemia: a pilot retrospective study in Chinese.

Zhang R, Wu Y, Wang X, Lu X, Li Y, Li S, Yan X. Zhang R, et al. Among authors: lu x. Int J Med Sci. 2020 Jan 18;17(3):325-331. doi: 10.7150/ijms.39307. eCollection 2020. Int J Med Sci. 2020. PMID: 32132867 Free PMC article.

10

Deletion of 14q24.1 approximately q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization.

Xu W, Lu X, Kim Y, Luo Y, Martin M, Mulvihill JJ, Li S. Xu W, et al. Among authors: lu x. Cancer Genet Cytogenet. 2008 Aug;185(1):43-6. doi: 10.1016/j.cancergencyto.2008.04.007. Cancer Genet Cytogenet. 2008. PMID: 18656693

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