A New Variant Translocation of t(15;17) in a Patient with Acute Promyelocytic Leukemia (M3): t(15;19;17)(q22;p13;q12)-Reference-Cited by-同舟云学术

A New Variant Translocation of t(15;17) in a Patient with Acute Promyelocytic Leukemia (M3): t(15;19;17)(q22;p13;q12)

Published:1998-04 Issue:1 Volume:102 Page:15-18
ISSN:0165-4608
Container-title:Cancer Genetics and Cytogenetics
language:en
Short-container-title:Cancer Genetics and Cytogenetics

Author:

Saitoh Kohki,Miura Ikuo,Kobayashi Yoshimi,Kume Masaaki,Utsumi Seiko,Takahashi Naoto,Hatano Yoshiaki,Nimura Takashi,Hashimoto Keiko,Takahashi Satsuki,Miura Akira B.

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference15 articles.

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2. Heim S, Mitelman F (1995): Cancer Cytogenetics, ed. 2. Wiley-Liss, New York, pp. 252–258.

3. Sandberg AA (1990): The Chromosomes in Human Cancer and Leukemia, ed. 2. Elsevier, New York.

4. ISCN (1995): An International System for Human Cytogenetic Nomenclature. F Mitelman, ed. S. Karger, Basel.

5. Molecular analysis of simple variant translocations in acute promyelocytic leukemia;Borrow;Genes Chromosom Cancer,1994

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1. A complex translocation (3;17;15) in acute promyelocytic leukemia confirmed by fluorescence in situ hybridization;Oncology Letters;2016-10-18

2. Coexistence of t(15;17) and t(15;16;17) detected by fluorescence in situ hybridization in a patient with acute promyelocytic leukemia: A case report and literature review;Oncology Letters;2014-07-02

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