Fig. 3From: Terminal microdeletion of chromosome 18 in a Malaysian boy characterized with few features of typical 18q- deletion syndrome: a case reportA phenotypic map of chromosome 18q indicating the critical regions for various clinical features. CAA congenital aural atresia, CP/CL cleft palate/cleft lip, MR mental retardation. The deletion presented in our patient is indicated by a red bar. Modified from [7]Back to article page