Neurobehavioral phenotype observed in KBG syndrome caused byANKRD11mutations

Familial 16q24.3 microdeletion involving ANKRD11 causes a KBG-like syndrome

(2012) Stephanie Sacharow et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A developmental and genetic classification for malformations of cortical development: update 2012

(2012) A. James Barkovich et al.   BRAIN

Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia

(2011) Asli Sirmaci et al.   AMERICAN JOURNAL OF HUMAN GENETICS

ANKRD11 gene deletion in a 17-year-old male

(2011) Erin L. Youngs et al.   CLINICAL DYSMORPHOLOGY

Haploinsufficiency of ANKRD11 causes mild cognitive impairment, short stature and minor dysmorphisms

(2011) Mala Isrie et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Role of MeCP2, DNA methylation, and HDACs in regulating synapse function

(2011) Ege T. Kavalali et al.   Journal of Neurodevelopmental Disorders

The ancient mammalian KRAB zinc finger gene cluster on human chromosome 8q24.3 illustrates principles of C2H2 zinc finger evolution associated with unique expression profiles in human tissues

(2010) Peter Lorenz et al.   BMC GENOMICS

Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome

(2009) Marjolein H Willemsen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Alterations in CDH15 and KIRREL3 in Patients with Mild to Severe Intellectual Disability

(2008) Kavita Bhalla et al.   AMERICAN JOURNAL OF HUMAN GENETICS