• Amplification of ERBB2, RARA, and TOP2A genes in a myelodysplastic syndrome transforming to acute myeloid leukemia
• Combined immunophenotyping and karyotyping in peripheral T cell lymphomas demonstrating different clonal and nonclonal chromosome aberrations in T helper cells
• Molecular cytogenetic detection of chromosomal breakpoints in T-cell receptor gene loci
• Monozygotic twins with Klinefelter syndrome (concordant) and systemic lupus erythematodes (discordant)
• Probable autosomal recessive syndrome with triphalangia of thumbs, thrombasthenia Glanzmann and deafness of internal ear