Genomic aberrations in mantle cell lymphoma detected by interphase fluorescence in situ hybridization. Incidence and clinicopathological correlations

Background The genetic hallmark of mantle cell lymphoma is a t(11;14)(q13;q32). However, additional genomic alterations are likely involved in the pathogenesis of this lymphoma.Design and Methods To determine the incidence and clinical relevance of these aberrations, we analyzed 103 well-characteriz...

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Библиографические подробности

Главные авторы:	Sandrine Sander, Lars Bullinger, Elke Leupolt, Axel Benner, Dirk Kienle, Tiemo Katzenberger, Jörg Kalla, German Ott, Hans Konrad Müller-Hermelink, Thomas F.E. Barth, Peter Möller, Peter Lichter, Hartmut Döhner, Stephan Stilgenbauer
Формат:	Artigo
Язык:	Inglês
Опубликовано:	Ferrata Storti Foundation 2008-05-01
Серии:	Haematologica
Online-ссылка:	https://haematologica.org/article/view/4840
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