• A 17q12 chromosomal duplication associated with renal disease and esophageal atresia
• Another case of t(17;22)(q22;q13) in an infantile dermatofibrosarcoma protuberans
• Chronic myelomonocytic leukemia with trisomy 8 and a related clone with trisomy 8 and t(15;17)
• Coexistence of tetrasomy 8 and trisomy 8 in acute promyelocytic leukemia (AML-M3) with t(15;17)(q22;q12)
• Cytogenetic studies in acute promyelocytic leukemia: a survey of secondary chromosomal abnormalities
• Derivative (7)t(7;8)(q34;q21). a new additional cytogenetic abnormality in acute promyelocytic leukemia
• Genomic abnormalities acquired in the blastic transformation of splenic marginal zone B-cell lymphoma
• Interstitial insertion of retinoic acid receptor-alpha gene in acute promyelocytic leukemia with normal chromosomes 15 and 17
• Myelodysplastic syndrome transforming to acute promyelocytic-like leukemia with trisomy and rearrangement of chromosome 11
• Non-immunologic hydrops fetalis (NIHF)--case report of double partial trisomy 15q and 17q resulting from familial translocation 15/17 and cytogenetic findings in 50 cases with hydrops fetalis
• Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qter
• Recurring chromosomal abnormalities in leukemia in PML-RARA transgenic mice parallel human acute promyelocytic leukemia
• Trisomy 21 and other chromosomal abnormalities in acute promyelocytic leukemia