|1.||Brancati, Francesco: 3 articles (02/2015 - 08/2011)|
|2.||Tekin, Mustafa: 2 articles (02/2015 - 08/2011)|
|3.||Curatolo, Paolo: 2 articles (02/2015 - 01/2013)|
|4.||Foster, Joseph: 1 article (02/2015)|
|5.||Callen, David F: 1 article (02/2015)|
|6.||Cho, Eunhae: 1 article (02/2015)|
|7.||Neilsen, Paul M: 1 article (02/2015)|
|8.||Verbeek, Nienke E: 1 article (02/2015)|
|9.||Bjørgo, Kathrine: 1 article (02/2015)|
|10.||Diaz-Horta, Oscar: 1 article (02/2015)|
|1.||Mental Retardation (Idiocy)
02/01/2015 - "As a result, we conclude that severe short stature, intellectual disability, and macrodontia are the main characteristics in KBG syndrome related to ANKRD11 mutation. "
02/01/2015 - "Mutations in ANKRD11 have recently been reported to cause KBG syndrome, an autosomal dominant condition characterized by intellectual disability (ID), behavioral problems, and macrodontia. "
01/01/2015 - "KBG syndrome is a rare disorder characterized by intellectual disability and associated with macrodontia of the upper central incisors, specific craniofacial findings, short stature and skeletal anomalies. "
05/01/2013 - "KBG syndrome is characterized by postnatal short stature, macrodontia, facial and hand anomalies, delayed bone age and intellectual disability. "
08/12/2011 - "KBG syndrome is characterized by intellectual disability associated with macrodontia of the upper central incisors as well as distinct craniofacial findings, short stature, and skeletal anomalies. "
|2.||Autistic Disorder (Autism)
09/01/2014 - "This patient provided additional evidence on the influence of ANKRD11 in KBG syndrome and suggested that deletion limited to ANKRD11 is unlikely to cause autism. "
12/01/2009 - "Twins with KBG syndrome and autism."
01/01/2013 - "Recently, mutations in ANKRD11 gene have been identified in a subset of patients with KBG syndrome, while a contiguous gene deletion syndrome involving 16q24.3 region (including ANKRD11) was delineated in patients with facial dysmorphism, autism, intellectual disability, and brain abnormalities. "
|3.||Rare Diseases (Rare Disease)
01/01/2013 - "KBG syndrome is a rare disease characterized by typical facial dysmorphism, macrodontia of upper central incisors, skeletal abnormalities, and developmental delay. "
02/01/2015 - "KBG syndrome is a rare disease characterized by intellectual disability, typical craniofacial dysmorphism, macrodontia of the upper central incisors, short stature, and skeletal anomalies. "
|4.||Periventricular Nodular Heterotopia