Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia: The American Journal of Human Genetics
A de novo frameshift variant of ANKRD11 (c.1366_1367dup) in a Chinese patient with KBG syndrome | BMC Medical Genomics | Full Text
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations | European Journal of Human Genetics
ANKRD11 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
KBG syndrome: Common and uncommon clinical features based on 31 new patients - Gnazzo - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Frontiers | The Chromatin Regulator Ankrd11 Controls Palate and Cranial Bone Development
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations | European Journal of Human Genetics
Autism gene guides early neuron development | Spectrum | Autism Research News
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
The KBGS flowchart. The figure summarizes the molecular diagnostic... | Download Scientific Diagram
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
Molecular characterization of the ANKRD11 intragenic duplication. (a)... | Download Scientific Diagram
IJMS | Free Full-Text | Expanding the Molecular Spectrum of ANKRD11 Gene Defects in 33 Patients with a Clinical Presentation of KBG Syndrome
ANKRD11 associated with intellectual disability and autism regulates dendrite differentiation via the BDNF/TrkB signaling pathway - ScienceDirect
Frontiers | Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review