Figure 1From: Chromosomal 16p microdeletion in Rubinstein-Taybi syndrome detected by oligonucleotide-based array comparative genomic hybridization: a case report Clinical features of our patient at the age of three years. Dysmorphic facial features include a prominent nasal bridge, hypertelorism and down-slanting palpebral fissures. Other features include (a) broad thumbs and fingers and (b) great toes.Back to article page