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Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG  Syndrome: Case Reports and Literature Review | Semantic Scholar
Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review | Semantic Scholar

Severity of intelligence disability (ID) and short stature (SS) in... |  Download Scientific Diagram
Severity of intelligence disability (ID) and short stature (SS) in... | Download Scientific Diagram

Clinical evaluation of individuals with ANKRD11 missense variants. A.... |  Download Scientific Diagram
Clinical evaluation of individuals with ANKRD11 missense variants. A.... | Download Scientific Diagram

ANKRD11 variants cause variable clinical features associated with KBG  syndrome and Coffin–Siris-like syndrome | Journal of Human Genetics
ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin–Siris-like syndrome | Journal of Human Genetics

Gene: ANKRD11 (ENSG00000167522) - Summary - Homo_sapiens - Ensembl genome  browser 109
Gene: ANKRD11 (ENSG00000167522) - Summary - Homo_sapiens - Ensembl genome browser 109

ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody

ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody

IJMS | Free Full-Text | Expanding the Molecular Spectrum of ANKRD11 Gene  Defects in 33 Patients with a Clinical Presentation of KBG Syndrome
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
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody

Some of the published mutations in ANKRD11, most of which are loss of... |  Download Scientific Diagram
Some of the published mutations in ANKRD11, most of which are loss of... | Download Scientific Diagram

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

ANKRD11 variants localization and genomic rearrangements (A) Genetic... |  Download Scientific Diagram
ANKRD11 variants localization and genomic rearrangements (A) Genetic... | Download Scientific Diagram

Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual  Disability, Skeletal Malformations, and Macrodontia: The American Journal  of Human Genetics
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
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
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
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
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
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
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
Autism gene guides early neuron development | Spectrum | Autism Research News

ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody

The KBGS flowchart. The figure summarizes the molecular diagnostic... |  Download Scientific Diagram
The KBGS flowchart. The figure summarizes the molecular diagnostic... | Download Scientific Diagram

ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody
ANKRD11 Gene - GeneCards | ANR11 Protein | ANR11 Antibody

Molecular characterization of the ANKRD11 intragenic duplication. (a)... |  Download Scientific Diagram
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
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
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
Frontiers | Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review