Duplication 15q as the sole anomaly in an acute promyelocytic leukemia patient without t(15;17)

We present a unique chromosomal abnormality found in a patient with acute myeloblastic leukemia of French–American–British subtype M3. The patient was referred for an evaluation of a chromosomal anomaly exclusively associated with FAB M3 or acute promyelocytic leukemia: a translocation between chrom...

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Veröffentlicht in:	Cancer genetics and cytogenetics 2002-10, Vol.138 (1), p.17-21
Hauptverfasser:	Zhang, Lijun, Mulvihill, John J, Kern, William F, McMinn, Johnny, Li, Shibo
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Biological and medical sciences Bone Marrow - pathology Chromosomes, Human, Pair 15 - genetics Chromosomes, Human, Pair 17 Gene Duplication Hematologic and hematopoietic diseases Humans In Situ Hybridization, Fluorescence Karyotyping Leukemia, Myeloid, Acute - genetics Leukemia, Myeloid, Acute - pathology Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Medical sciences Translocation, Genetic
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