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Molecular characterization of the region 7q22.1 in splenic marginal zone lymphomas.Integration of global spectral karyotyping, CGH arrays, and expression arrays reveals important genes in the pathogenesis of glioblastoma multiforme.A Low Frequency of Losses in 11q Chromosome Is Associated with Better Outcome and Lower Rate of Genomic Mutations in Patients with Chronic Lymphocytic Leukemia.Genome-Wide DNA Copy Number Analysis of Acute Lymphoblastic Leukemia Identifies New Genetic Markers Associated with Clinical Outcome.Chromothripsis Is a Recurrent Genomic Abnormality in High-Risk Myelodysplastic Syndromes.Next-generation sequencing and FISH studies reveal the appearance of gene mutations and chromosomal abnormalities in hematopoietic progenitors in chronic lymphocytic leukemia.Onychomatricoma: genome-wide analyses of a rare nail matrix tumor.Hyperdiploidy as a rare event that accompanies poor prognosis markers in CLL.Bone marrow fibrosis in myelodysplastic syndromes: a prospective evaluation including mutational analysis.Multidimensional assessment of patient condition and mutational analysis in peripheral blood, as tools to improve outcome prediction in myelodysplastic syndromes: A prospective study of the Spanish MDS group.MiRNA expression profile of chronic lymphocytic leukemia patients with 13q deletion.Array comparative genomic hybridization identifies genetic regions associated with outcome in aggressive diffuse large B-cell lymphomas.Calreticulin mutations are exceedingly rare in patients with myelodysplastic syndromes with myelofibrosis.Expression of VAV1 in the tumour microenvironment of glioblastoma multiforme.Mutations in TP53 and JAK2 are independent prognostic biomarkers in B-cell precursor acute lymphoblastic leukaemia.A two-step approach for sequencing spliceosome-related genes as a complementary diagnostic assay in MDS patients with ringed sideroblasts.SLUG (SNAI2) overexpression in embryonic development.Genomic analysis of clonal eosinophils by CGH arrays reveals new genetic regions involved in chronic eosinophilia.Identification of a novel recurrent gain on 20q13 in chronic lymphocytic leukemia by array CGH and gene expression profilingImatinib therapy of chronic myeloid leukemia restores the expression levels of key genes for DNA damage and cell-cycle progressionChromosomal abnormalities are related to location and grade of osteoarthritisAnalysis of chromosomal imbalances in an elderly woman with a giant cell tumourBoth expanded and uncultured mesenchymal stem cells from MDS patients are genomically abnormal, showing a specific genetic profile for the 5q- syndromeThe presence of genomic imbalances is associated with poor outcome in patients with burkitt lymphoma treated with dose-intensive chemotherapy including rituximabFrequency of low-level and high-level mosaicism in sporadic retinoblastoma: genotype-phenotype relationships
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description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Cristina Robledo
@ast
Cristina Robledo
@en
Cristina Robledo
@es
Cristina Robledo
@nl
Cristina Robledo
@sl
type
label
Cristina Robledo
@ast
Cristina Robledo
@en
Cristina Robledo
@es
Cristina Robledo
@nl
Cristina Robledo
@sl
prefLabel
Cristina Robledo
@ast
Cristina Robledo
@en
Cristina Robledo
@es
Cristina Robledo
@nl
Cristina Robledo
@sl
P108
P106
P1153
14009579000
P21
P31
P496
0000-0003-0445-3210