Haploinsufficiency of ANKRD11 causes mild cognitive impairment, short stature and minor dysmorphisms | European Journal of Human Genetics
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
Genes | Free Full-Text | Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving
Molecular characterization of the ANKRD11 intragenic duplication. (a)... | Download Scientific Diagram
ANKRD11 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
Frontiers | SETD5 Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome
Frontiers | Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review
Frontiers | Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations | European Journal of Human Genetics
Some of the published mutations in ANKRD11, most of which are loss of... | Download Scientific Diagram
Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia - ScienceDirect
ANKRD11 associated with intellectual disability and autism regulates dendrite differentiation via the BDNF/TrkB signaling pathway - ScienceDirect
Gene: ANKRD11 (ENSG00000167522) - Summary - Homo_sapiens - Ensembl genome browser 109
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
A de novo frameshift variant of ANKRD11 (c.1366_1367dup) in a Chinese patient with KBG syndrome | BMC Medical Genomics | Full Text
IJMS | Free Full-Text | Expanding the Molecular Spectrum of ANKRD11 Gene Defects in 33 Patients with a Clinical Presentation of KBG Syndrome
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report | BMC Medical Genetics | Full Text
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
