Intellectual Profiles in KBG-Syndrome: A Wechsler Based Case-Control Study

Author:

van Dongen Linde C. M.,Wingbermühle Ellen,Oomens Wouter,Bos-Roubos Anja G.,Ockeloen Charlotte W.,Kleefstra Tjitske,Egger Jos I. M.

Publisher

Frontiers Media SA

Subject

Behavioral Neuroscience,Cognitive Neuroscience,Neuropsychology and Physiological Psychology

Reference23 articles.

1. KBG syndrome in a cohort of Italian patients;Brancati;Am. J. Med. Genet. A,2004

2. Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation of ANKRD11;Goldenberg;Am. J. Med. Genet. A,2016

3. Twins with KBG syndrome and autism;Hah;J. Autism Dev. Disord.,2009

4. The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies;Herrmann;Birth Defects Orig. Artic. Ser.,1975

5. A Korean family with KBG syndrome identified by ANKRD11 mutation, and phenotypic comparison of ANKRD11 mutation and 16q24.3 microdeletion;Kim;Eur. J. Med. Genet.,2015

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