Lista de obras -

14q deletions are associated with trisomy 12,NOTCH1mutations and unmutatedIGHVgenes in chronic lymphocytic leukemia and small lymphocytic lymphoma

artículo científico publicado en 2014

Contribution of MLPA to routine diagnostic testing of recurrent genomic aberrations in chronic lymphocytic leukemia.

artículo científico publicado en 2013

De novo 2q36.1q36.3 interstitial deletion involving the PAX3 and EPHA4 genes in a fetus with spina bifida and cleft palate.

artículo científico publicado en 2014

De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features.

artículo científico publicado en 2010

ERCC1 and telomere status in breast tumours treated with neoadjuvant chemotherapy and their association with patient prognosis

artículo científico publicado en 2016

Familial deletion 11q14.3-q22.1 without apparent phenotypic consequences: a haplosufficient 8.5 Mb region

article

Gain of the short arm of chromosome 2 (2p) is a frequent recurring chromosome aberration in untreated chronic lymphocytic leukemia (CLL) at advanced stages

article

Gene dosage methods as diagnostic tools for the identification of chromosome abnormalities.

artículo científico publicado en 2008

Interleukin-6 gene amplification and shortened survival in glioblastoma patients.

artículo científico publicado en 2007

Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p

artículo científico publicado en 2008

Low MCL-1 mRNA expression correlates with prolonged survival in B-cell chronic lymphocytic leukemia

scientific article published on 29 November 2007

Outcome and impact of post-remission strategy after MIDAM regimen in patients with relapsing or refractory acute myeloid leukemia

artículo científico publicado en 2018

Poor prognosis of chromosome 7 clonal aberrations in Philadelphia-negative metaphases and relevance of potential underlying myelodysplastic features in chronic myeloid leukemia

artículo científico publicado en 2018

Prenatal detection of cryptic rearrangements by multiplex ligation probe amplification in fetuses with ultrasound abnormalities.

artículo científico publicado en 2010

Prenatal ultrasound diagnosis of a 48,XXYY syndrome.

artículo científico publicado en 2013

Presence of multiple recurrent mutations confers poor trial outcome of relapsed/refractory CLL.

artículo científico publicado en 2015

Strong correlation between VEGF and MCL-1 mRNA expression levels in B-cell chronic lymphocytic leukemia.

artículo científico publicado en 2009

TERT promoter status and gene copy number gains: effect on TERT expression and association with prognosis in breast cancer

artículo científico publicado en 2017

Telomere status in chronic lymphocytic leukemia with TP53 disruption.