Types of frontonasal dysplasia (type 14 cleft) due to mutations in cartilage-specific homeoproteins

Reproduced from: Uz E, Alanay Y, Aktas D, et al. Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: Expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia. Am J Hum Genet 2010; 86:789. Illustration used with the permission of Elsevier Inc. All rights reserved.