Genotypes and phenotypes of the 16 previously identified cases of 1q25-32deletions. The locations of deletions are listed in the left. Deletions confirmed by molecular methods are illustrated with solid horizontal lines and unconfirmed deletions with dotted line. Phenotypes of each deletion are listed in right box. GR, growth retardation; PR, psychomotor retardation; L/P, lip/palate anomalies; GA, genital abnormalities; H/F, small hands/feet; BD, brachydactyly; CL, fifth finger clinodactyly; CA, cardiac anomalies; MC, microcephaly; MG, micrognathia; +, positive; -, negative; NA, no available; P, patient.