SNPs Array Karyotyping Reveals a Novel Recurrent 20p13 Amplification in Primary Myelofibrosis

The molecular pathogenesis of primary mielofibrosis (PMF) is still largely unknown. Recently, single-nucleotide polymorphism arrays (SNP-A) allowed for genome-wide profiling of copy-number alterations and acquired uniparental disomy (aUPD) at high-resolution. In this study we analyzed 20 PMF patient...

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Detalles Bibliográficos
Autores principales: Visani, Giuseppe, Sapienza, Maria Rosaria, Isidori, Alessandro, Tripodo, Claudio, Laginestra, Maria Antonella, Righi, Simona, Sagramoso Sacchetti, Carlo A., Gazzola, Anna, Mannu, Claudia, Rossi, Maura, De Nictolis, Michele, Valentini, Massimo, Donati, Meris, Emiliani, Roberto, Alesiani, Francesco, Paolini, Stefania, Finelli, Carlo, Pileri, Stefano A., Piccaluga, Pier Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215741/
https://www.ncbi.nlm.nih.gov/pubmed/22110671
http://dx.doi.org/10.1371/journal.pone.0027560

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215741/
https://www.ncbi.nlm.nih.gov/pubmed/22110671
http://dx.doi.org/10.1371/journal.pone.0027560

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