Coté G B, Papadakou-Lagoyanni S, Kairis M
Ann Genet. 1980;23(3):171-2.
Fryns and his colleagues described two children with a remarkably similar phenotype, and suggested their condition was due to a partial or total deletion of the long arm of chromosome 16 distal to band q21. We report the same phenotype in a boy whose blood karyotype was normal.
