Title of article
Fluorescence In Situ Hybridization Characterization of the Chromosomal Breakpoints in a Case with ins(17;3)(q11.2;q21q26.3) and Acute Monocytic Leukemia
Author/Authors
Schnittger، نويسنده , , Susanne and Joachimmayer، نويسنده , , Elke and Schoch، نويسنده , , Claudia and Fuchs، نويسنده , , Roland and Fonatsch، نويسنده , , Christa، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1998
Pages
6
From page
122
To page
127
Abstract
A 63-year-old patient with acute myeloid leukemia of FAB M5 subtype revealing chromosomal breakpoints in 3q21 and 3q26 is presented. Although rearrangements of 3q21 and 3q26 are relatively common in patients with myelocytic malignancies, this is the first report of ins(17;3)(q11.2; q21q26.3). We defined the chromosomal breakpoints and the extent of the insertion by fluorescence in situ hybridization (FISH) with yeast artificial chromosomes (YACs).
Journal title
Cancer Genetics and Cytogenetics
Serial Year
1998
Journal title
Cancer Genetics and Cytogenetics
Record number
1821498
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