• A Peculiar CLL Case with Complex Chromosome 6 Rearrangements and Refinement of All Breakpoints at the Gene Level by Genomic Array: A Case Report
• A pure familial 6q15q21 split duplication associated with obesity and transmitted with partial reduction
• An Adolescent with a Rare <em>De Novo</em> Distal Trisomy 6p and Distal Monosomy 6q Chromosomal Combination
• Cytogenetic and molecular characterization of a patient with partial 6q trisomy and 1q monosomy
• Evolution of multiple cell clones over a 29-year period of a CLL patient
• Exome and genome sequencing to unravel the precise breakpoints of partial trisomy 6q and partial Monosomy 2q
• Gene mutations connected to Waldenstöm macroglobulinemia
• Improved identification for trisomy 9p and partial trisomy 6q presented in a patient by array-based comparative genomic hybridization
• Mitotic recombinatory evolution in acute leukemia
• Molecular cytogenetic characterisation of a novel <em>de novo</em> ring chromosome 6 involving a terminal 6p deletion and terminal 6q duplication in the different arms of the same chromosome
• Mosaic 46,XY,der(15)t(6;15)(q25.1;p12)/46,XY at amniocentesis in a pregnancy associated with a favorable fetal outcome and postnatal decrease of the aneuploid cell line with the unbalanced translocation
• Oligo-based aCGH analysis reveals cryptic unbalanced der(6)t(X;6) in pediatric t(12;21)-positive acute lymphoblastic leukemia
• Prenatal diagnosis and ultrasonographic findings of partial trisomy of chromosome 6q: A case report and review of the literature
• Prenatal diagnosis for a pedigree affected with Wolf-Hirschhorn syndrome due to a subtle chromosomal translocation
• Pure interstitial dup(6)(q22.31q22.31) - a case report
• Recurrent Cytogenetic Abnormalities in Intravascular Large B-Cell Lymphoma
• Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series