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Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1–PRDM16 fusion in a case of progressive chronic myeloid leukemia: A complex chromosomal rearrangement of underestimated frequency in disease progression?

✍ Scribed by Lauréline Deluche; Sami Joha; Sélim Corm; Agnès Daudignon; Sandrine Geffroy; Sabine Quief; Céline Villenet; Jean-Pierre Kerckaert; Jean-Luc Laï; Claude Preudhomme; Catherine Roche-Lestienne

Book ID: 118283666
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 405 KB
Volume: 47
Category: Article
ISSN: 1045-2257
DOI: 10.1002/gcc.20611

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