TY  - JOUR
AU  - Abáigar, María
AU  - Robledo, Cristina
AU  - Benito, Rocío
AU  - Ramos, Fernando
AU  - Díez-Campelo, María
AU  - Hermosín, Lourdes
AU  - Sánchez-Del-Real, Javier
AU  - Alonso, Jose M
AU  - Cuello, Rebeca
AU  - Megido, Marta
AU  - Rodríguez, Juan N
AU  - Martín-Núñez, Guillermo
AU  - Aguilar, Carlos
AU  - Vargas, Manuel
AU  - Martín, Ana A
AU  - García, Juan L
AU  - Kohlmann, Alexander
AU  - Del Cañizo, M Consuelo
AU  - Hernández-Rivas, Jesús M
PY  - 2016
DO  - 10.1371/journal.pone.0164370
UR  - http://hdl.handle.net/10668/10536
T2  - PloS one
AB  - To explore novel genetic abnormalities occurring in myelodysplastic syndromes (MDS) through an integrative study combining array-based comparative genomic hybridization (aCGH) and next-generation sequencing (NGS) in a series of MDS and...
LA  - en
KW  - Adolescent
KW  - Adult
KW  - Aged
KW  - Aged, 80 and over
KW  - Child
KW  - Chromosome Aberrations
KW  - Chromosomes, Human, Pair 13
KW  - Comparative Genomic Hybridization
KW  - Core Binding Factor Alpha 2 Subunit
KW  - DNA
KW  - DNA (Cytosine-5-)-Methyltransferases
KW  - DNA Copy Number Variations
KW  - DNA Methyltransferase 3A
KW  - DNA Mutational Analysis
KW  - DNA-Binding Proteins
KW  - Dioxygenases
KW  - Female
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Karyotype
KW  - Male
KW  - Middle Aged
KW  - Myelodysplastic Syndromes
KW  - Proto-Oncogene Proteins
KW  - Recurrence
KW  - Risk
KW  - Tumor Suppressor Protein p53
KW  - Young Adult
TI  - Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes.
TY  - research article
VL  - 11
ER  -