ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
Severity of intelligence disability (ID) and short stature (SS) in... | Download Scientific Diagram
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations | European Journal of Human Genetics
ANKRD11 variants localization and genomic rearrangements (A) Genetic... | Download Scientific Diagram
KBG syndrome: Common and uncommon clinical features based on 31 new patients - Gnazzo - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
Frontiers | The Chromatin Regulator Ankrd11 Controls Palate and Cranial Bone Development
ANKRD11 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
IJMS | Free Full-Text | Expanding the Molecular Spectrum of ANKRD11 Gene Defects in 33 Patients with a Clinical Presentation of KBG Syndrome
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
IJMS | Free Full-Text | Expanding the Molecular Spectrum of ANKRD11 Gene Defects in 33 Patients with a Clinical Presentation of KBG Syndrome
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations | European Journal of Human Genetics
ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin–Siris-like syndrome | Journal of Human Genetics
Haploinsufficiency for ANKRD11-flanking genes makes the difference between KBG and 16q24.3 microdeletion syndromes: 12 new cases | European 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
ANKRD11 associated with intellectual disability and autism regulates dendrite differentiation via the BDNF/TrkB signaling pathway - ScienceDirect
Genetic and Phenotypic Spectrum of KBG Syndrome: A Report of 13 New Chinese Cases and a Review of the Literature
Haploinsufficiency of ANKRD11 causes mild cognitive impairment, short stature and minor dysmorphisms | European Journal of Human Genetics
What causes Cornelia de Lange Syndrome - CdLS Foundation UK and Ireland
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
ANKRD11 variants: KBG syndrome and beyond - Parenti - 2021 - Clinical Genetics - Wiley Online Library
Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia - ScienceDirect
