Exploring the behavioral and cognitive phenotype of KBG syndrome

KBG syndrome is a neurodevelopmental disorder, caused by dominant mutations in ANKRD11, that is characterized by developmental delay/intellectual disability, mild craniofacial dysmorphisms, and short stature. Behavior and cognition have hardly been studied, but anecdotal evidence suggests higher fre...

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Detalles Bibliográficos
Autores principales: van Dongen, Linde C.M., Wingbermühle, Ellen, van der Veld, William M., Vermeulen, Karlijn, Bos‐Roubos, Anja G., Ockeloen, Charlotte W., Kleefstra, Tjitske, Egger, Jos I.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850621/
https://www.ncbi.nlm.nih.gov/pubmed/30786142
http://dx.doi.org/10.1111/gbb.12553

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850621/
https://www.ncbi.nlm.nih.gov/pubmed/30786142
http://dx.doi.org/10.1111/gbb.12553

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