Secondary Logo

Journal Logo

July 2003 - Volume 12 - Issue 3
pp: 153-213

A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features

Oktenli, Cagatay; Saglam, Mutlu; Demirbas, Seref; More

Clinical Dysmorphology. 12(3):199-201, July 2003.