ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
Frontiers | The Chromatin Regulator Ankrd11 Controls Palate and Cranial Bone Development
Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia: The American Journal of Human Genetics
Clinical evaluation of individuals with ANKRD11 missense variants. A.... | Download Scientific Diagram
Genetic and Phenotypic Spectrum of KBG Syndrome: A Report of 13 New Chinese Cases and a Review of the Literature
A) Electropherograms of the patient 1 and his parents. A de novo... | Download Scientific Diagram
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia - ScienceDirect
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
Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations | European Journal of Human Genetics
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
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
ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin–Siris-like syndrome | Journal of Human Genetics
Frontiers | Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review
Haploinsufficiency for ANKRD11-flanking genes makes the difference between KBG and 16q24.3 microdeletion syndromes: 12 new cases | European Journal of Human Genetics
Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review | Semantic Scholar
Autism gene guides early neuron development | Spectrum | Autism Research News
Haploinsufficiency of ANKRD11 causes mild cognitive impairment, short stature and minor dysmorphisms | European Journal of Human Genetics
ANKRD11 variants: KBG syndrome and beyond - Parenti - 2021 - Clinical Genetics - Wiley Online Library
ANKRD11 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
Some of the published mutations in ANKRD11, most of which are loss of... | 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
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
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
