• Fine-needle aspiration biopsy of uveal melanoma: outcomes and complications
• Mild phenotypic abnormalities in combined del 9p2 and dup 3p2
• Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy
• Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization
• Three Japanese patients with 3p13 microdeletions involving FOXP1