Feldman G M, Baumer J G, Sparkes R S
Am J Med Genet. 1982 Mar;11(3):299-304. doi: 10.1002/ajmg.1320110306.
In a 42-month-old girl a duplicated 17p chromosome anomaly was identified by trypsin-Giemsa banding techniques. The clinical findings are compared with those of previous case reports. Common phenotypics changes include failure to thrive; hypoplastic, apparently low-set ears; micrognathia; flexion abnormalities of fingers; and foot abnormalities.
