Bai SX - Search Results

1

[Fluorescence in situ hybridization studies on a myeloid leukemia patient with ins(8;21)(q22;q22.1q22.3)].

Wu YF, Xue YQ, Bai SX, Zhang J, Yao L, Wang Y, Qiu HY, Shen J, Pan JL, Ma QF. Wu YF, et al. Among authors: bai sx. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Apr;26(2):203-6. doi: 10.3760/cma.j.issn.1003-9406.2009.02.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19350517 Chinese.

2

[Fluorescence in situ hybridization study of acute myeloid leukemia with cryptic chromosome rearrangements].

Bai SX, Xue YQ, Chen SN, Pan JL, Wu YF, Shen J, Wang Y, Zhang J. Bai SX, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):690-3. doi: 10.3760/cma.j.issn.1003-9406.2011.06.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 22161107 Chinese.

3

[Clinical and experimental study of a multiple myeloma case with low hypodiploidy].

Bai SX, Pan JL, Xue YQ, Chen SN, Wu YF, Wang Y, Zhang J, Shen J. Bai SX, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Jun;29(3):343-6. doi: 10.3760/cma.j.issn.1003-9406.2012.03.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22678804 Chinese.

4

[Clinical and cytogenetic study of 6 cases of hematological disorders associated with 20q- and t (20;21) (q11;q11) abnormalities].

Wu CX, Pan JL, Qiu HY, Xue YQ, Chen SN, Zhang J, Wu YF, Shen J, Bai SX, Wang Y. Wu CX, et al. Among authors: bai sx. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Apr;30(2):138-42. doi: 10.3760/cma.j.issn.1003-9406.2013.04.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23568721 Chinese.

5

[Clinical Significance of Common Gene Mutations in 53 Patients with Acute Myeloid Leukemia Harboring 11q23/MLL Rearrangements].

Bai SX, Gong YL, Zhang JR, Wu CX, Zhang J, Qiu HY, Shen HJ, Cen JN, Chen SN, Pan JL. Bai SX, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Jun;28(3):717-723. doi: 10.19746/j.cnki.issn.1009-2137.2020.03.001. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020. PMID: 32552926 Chinese.

6

Translocation (14;14)(q11;q32) with simultaneous involvement of the IGH and CEBPE genes in B-lineage acute lymphoblastic leukemia.

Han Y, Xue Y, Zhang J, Wu Y, Pan J, Wang Y, Shen J, Dai H, Bai S. Han Y, et al. Cancer Genet Cytogenet. 2008 Dec;187(2):125-9. doi: 10.1016/j.cancergencyto.2008.08.008. Cancer Genet Cytogenet. 2008. PMID: 19027493

7

[Simultaneous presence of ins (15;17),t(2;17;20) and trisomy 8 in a patient with acute promyelocytic leukemia].

Bai S, Xue Y, Wu Y, Pan J, Zhang J, Shen J, Wang Y, Qiu H. Bai S, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):712-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065540 Chinese.

8

Y-chromosome loss as the sole karyotypic anomaly with 3'RARalpha submicroscopic deletion in a case of M3r subtype of acute promyelocytic leukemia.

Han Y, Xue Y, Zhang J, Pan J, Wu Y, Bai S. Han Y, et al. Leuk Res. 2009 Oct;33(10):1433-5. doi: 10.1016/j.leukres.2008.11.026. Epub 2009 Jan 6. Leuk Res. 2009. PMID: 19128831

9

[Chromosome study on chronic lymphocytic leukemia using CpG-oligodeoxynucleotide as immunostimulant agent].

Wu Y, Xue Y, Chen S, Yao L, Jiang H, Zhang J, Shen J, Pan J, Wang Y, Bai S. Wu Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Feb;27(1):86-91. doi: 10.3760/cma.j.issn.1003-9406.2010.01.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20140876 Chinese.

10

The utility of fluorescence in situ hybridization analysis in diagnosing myelodysplastic syndromes is limited to cases with karyotype failure.

Jiang H, Xue Y, Wang Q, Pan J, Wu Y, Zhang J, Bai S, Wang Q, He G, Sun A, Wu D, Chen S. Jiang H, et al. Leuk Res. 2012 Apr;36(4):448-52. doi: 10.1016/j.leukres.2011.10.014. Epub 2011 Nov 1. Leuk Res. 2012. PMID: 22047706

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