Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference23 articles.
1. The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies;Herrmann;Birth Defects Orig. Artic. Ser.,1975
2. The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype;Tekin;Am. J. Med. Genet.,2004
3. Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia;Sirmaci;Am. J. Hum. Genet.,2011
4. Familial 16q24.3 microdeletion involving ANKRD11 causes a KBG-like syndrome;Sacharow;Am. J. Med. Genet.,2012
5. KBG syndrome;Morel Swols;Orphanet J. Rare Dis.,2017