- Spectrin Tunis (Sp alpha I/78) in a Korean Family with Hereditary Elliptocytosis
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Han E, Kim A, Park J, Kim M, Kim Y, Han K, Kim YJ
- KMID: 1781350
- Ann Lab Med.
- 2013 Sep;33(5):386-389.
- doi: 10.3343/alm.2013.33.5.386
No abstract available. -
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- Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G
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Kim MS, Cho YU, Jang S, Seo EJ, Im HJ, Park CJ
- KMID: 2373636
- Ann Lab Med.
- 2017 Mar;37(2):162-165.
- doi: 10.3343/alm.2017.37.2.162
No abstract available. -
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- A Case of Therapy-Related Acute Leukemia With Mixed Phenotype With BCR-ABL1 After Treatment of Diffuse Large B-Cell Lymphoma
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Yang D, Cho SR, Jung S, Lee W, Hwang HY, Lee HS, Kim YS, Choi JR, Kim MH
- KMID: 2373637
- Ann Lab Med.
- 2017 Mar;37(2):166-168.
- doi: 10.3343/alm.2017.37.2.166
No abstract available. -
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- A Case of Adult B Lymphoblastic Leukemia with ider(9)(q10)t(9;22)(q34;q11.2) and der(19)t(1;19)(q23;p13.3)
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Jung SI, Cho HS, Lee CH, Jung BC
- KMID: 1781663
- Korean J Lab Med.
- 2010 Dec;30(6):585-590.
- doi: 10.3343/kjlm.2010.30.6.585
In B lymphoblastic leukemia/lymphoma (B-ALL/LBL), t(9;22)(q34;q11.2) and t(1;19)(q23;p13.3) are recurrent cytogenetic abnormalities. The concurrent occurrence of both abnormalities is very rare, and only 3 cases have been previously reported. Here,... -
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