Care pathways in childhood neurodevelopmental disorders: Toward greater awareness of KBG syndrome among pediatricians

Author:

Adamo-Croux MarieORCID,Auger-Gilli AdrianeORCID,Guyader Gwenaël Le,Aubin-Courjault Juliette,Margot HenriORCID,Bar ClaireORCID,Lacombe Didier,Van-Gils JulienORCID,Legendre Marine,Binet AurélienORCID,Horn Xavier Le GuillouORCID

Publisher

Elsevier BV

Reference27 articles.

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

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