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Deletion of chromosome 15 represents a rare but recurrent chromosomal abnormality in myelocytic malignancies

✍ Scribed by Judith Dierlamm; Georgia Schilling; Lucienne Michaux; Kristina Hinz; Eva Maria Murga Penas; Doris Seeger; Anne Hagemeijer; Dieter Kurt Hossfeld

Book ID: 114135562
Publisher: Elsevier Science
Year: 2003
Tongue: English
Weight: 150 KB
Volume: 144
Category: Article
ISSN: 0165-4608
DOI: 10.1016/s0165-4608(02)00863-4

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## Abstract __MLL__ gene rearrangements leading to production of MLL fusion proteins are commonly detected in infant leukemia patients; the most common __MLL__ fusion associated with infant leukemia is the __MLL‐AF4__ fusion. A single case of chromosomal rearrangement leading to production of an __