> A der(11)t(4;11)(q21;p15) in a T-ALLLBL patient

> An unusual translocation, t(1;11)(q21;q23), in a case of chronic myeloid leukemia with a cryptic Philadelphia chromosome

> Association of Distal Deletion of the Short arm of Chromosome 9 with

> Case Report Description of a Patient with Trisomy 22 in inbred line

> Genomic imbalances and microRNA transcriptional profiles in patients with mycosis fungoides.

> Phenotypic variability in 47, XXX patients.

> Progression of chromosomal damage induced by etoposide

> Cytogenomic Characterization of Chromosomal X-1 Translocation to Establish a More Accurate Phenotype-Genotype Correlation in an Adolescent with Primary Ovarian Insufficiency

> SOX11 expression in chronic lymphocytic leukemia correlates with adverse prognostic markers

> Telomere shortening associated with increased genomic complexity in chronic lymphocytic leukemia.

> Molecular alterations in the integrated diagnosis of pediatric glial and glioneuronal tumors: A single center experience

> A new dual translocation of chron1osome 14 in a pediatric Burkitt lymphon1a/leukemia patient: t(8;14) and t(14;15)

> Aplicación de Hibridación In Situ Fluorescente (FISH) en pacientes con sospecha clínica de Síndrome de Deleción 22q11.2 (SD22q11.2)

> Inversiones cromosómicas (anomalías estructurales poco frecuentes) asociadas a fenotipo normal, dudoso y patológico

> First sex modification case in equine cloning