• Concurrence of dominant piebald trait and fragile X syndrome
• Eye abnormalities in the Smith-Magenis contiguous gene deletion syndrome
• Mosaicism for deletion 17p11.2 in a boy with the Smith-Magenis syndrome
• New mental retardation syndrome with hearing impairment, distinct facial appearance, and skeletal anomalies
• The spasmodic upper-body squeeze: a characteristic behavior in Smith-Magenis syndrome