A complex translocation t(2;17;15) (q13:q21:q22) in a patient with acute promyelocytic leukemia(Abstracts of the 49th Annual Meeting of the Society of Chromosome Research)
スポンサーリンク
概要
著者
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Oshimi Kazuo
Div. Hematol. School Med. Juntendo Univ.
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OKADA Michiko
Chromosome Lab., Shiseikai Dai-Ni Hosp.
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Okada Michiko
Chromosome Lab. Shiseikai Dai-ni Hosp.
関連論文
- A complex translocation t(2;17;15) (q13:q21:q22) in a patient with acute promyelocytic leukemia(Abstracts of the 49th Annual Meeting of the Society of Chromosome Research)
- O-29. Chromosome 13 monosomy in multiple myeloma : Interphase FISH studies and karyotype analyses(Abstracts for the oral and the poster presentations,Abstracts of the Joint Meeting: the 58th Annual Meeting of the Society of Chromosome Research and the 17t
- O-26. t(11;14)(q13;q32) in malignant monoclonal gammopathies : Interphase FISH studies and karyotype analyses(Abstracts of the oral and poster presentations, Abstract of the 56th Annual Meeting of The Society of Chromosome Research)
- Delineation of the Frequently Deleted Region on Chromosome Arm 13q in B-cell Non-Hodgkin's Lymphoma
- Detection of complex translocation, t(9;22;17;8;19)(q34;q11;p13;q24.3;q13.3), in a patient with chronic myeloid leukemia by fluorescence in situ hybridization(Abstracts of the 48th Annual Meeting of the Society of Chromosome Research)
- P-13. dic(1;15) and der(15)t(1;15), a type of 1q trisomy in myeloid disorders(Abstracts of the oral and poster presentations)
- Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20