• A nine-month-old boy with isodicentric chromosome 15: a case report
• A novel coexistence of tetrasomy 8 and FLT3-ITD along with variant 3 way translocation t(4;17;15) in acute promyelocytic leukemia: Case study and literature review
• A study of two Chinese patients with tetrasomy and pentasomy 15q11q13 including Prader-Willi/Angelman syndrome critical region present with developmental delays and mental impairment
• Complex de novo chromosomal rearrangement at 15q11-q13 involving an intrachromosomal triplication in a patient with a severe neuropsychological phenotype: clinical report and review of the literature
• Confluent and reticulated papillomatosis associated with 15q tetrasomy syndrome
• Maternal 15q Duplication Syndrome
• Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome
• Mosaic 15q duplication syndrome (tetrasomy 15q11.1-q13.2) in a child with behavior disorders: case report
• Neurological features and long-term follow-up in 15q11.2-13.1 duplication
• Nonmosaic tetrasomy 15q25.2 → qter identified with SNP microarray in a patient with characteristic facial appearance and review of the literature
• Nonmosaic tetrasomy 15q25.2 qter identified with SNP microarray in a patient with characteristic facial appearance and review of the literature
• Partial tetrasomy of the proximal long arm of chromosome 15 in two patients: the significance of the gene dosage in terms of phenotype
• Prenatal diagnosis of a de novo tetrasomy 15q24.3-25.3: Case report and literature review
• Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder
• Typical, atypical and cryptic t(15;17)(q24;q21) (PML::RARA) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual-color dual-fusion FISH studies
• Variable behavioural phenotypes of patients with monosomies of 15q26 and a review of 16 cases