1. Clinical and genetic aspects of KBG syndrome;Low;Am J Med Genet A,2016
2. The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies;Herrmann;Birth Defects Orig Artic Ser,1975
3. Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia;Sirmaci;Am J Hum Genet,2011
4. Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations;Ockeloen;Eur J Hum Genet EJHG,2015
5. Ankrd11 is a chromatin regulator involved in autism that is essential for neural development;Gallagher;Dev Cell,2015