Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO

Keyphrases

• Congenital Heart Defects 100%
• Gain-of-function mutation 100%
• Left Ventricular Noncompaction 100%
• Intellectual Disability 75%
• Developmental Delay 50%
• DNA Repair 25%
• Cardiomyopathy 25%
• Environmental Factors 25%
• Genetic Factors 25%
• RNA Synthesis 25%
• RNA-DNA 25%
• Transcriptional Regulation 25%
• Human Subjects 25%
• DNA-binding Proteins 25%
• Epigenetic Factors 25%
• Cardiac Transplantation 25%
• Phenotypic Outcome 25%
• Brain Imaging 25%
• Male Infant 25%
• Penetrance 25%
• Dysmorphic Features 25%
• Octamer 25%
• Clinical Database 25%
• Structural Defects 25%
• Ventricular Septal Defect 25%
• Atrial Septal Defect 25%
• Corpus Callosum 25%
• RNA Binding 25%
• Asymptomatic Pregnant Women 25%
• Single-gene Deletion 25%
• POU Domain 25%
• Exome Sequencing 25%
• Small Families 25%
• Relative Macrocephaly 25%
• Congenital Brain Anomalies 25%
• Stochastic Factors 25%
• CNV Analysis 25%
• Global Developmental Delay 25%

Medicine and Dentistry

• Congenital Heart Defect 100%
• Noncompaction Cardiomyopathy 100%
• Developmental Delay 75%
• Intellectual and Developmental Disabilities 75%
• DNA Repair 25%
• Gene Deletion 25%
• RNA Synthesis 25%
• Human Subject 25%
• DNA RNA Hybridization 25%
• Heart Transplantation 25%
• Brain Imaging 25%
• RNA Binding 25%
• Dysmorphic Feature 25%
• Macrocephaly 25%
• Exome Sequencing 25%
• DNA Binding Protein 25%
• Penetrance 25%
• Brain Malformation 25%
• Corpus Callosum 25%
• Myocardial Disease 25%

Biochemistry, Genetics and Molecular Biology

• Intellectual Disability 100%
• DNA Repair 33%
• Genetics 33%
• RNA Synthesis 33%
• Epigenetics 33%
• Gene Deletion 33%
• DNA RNA Hybridization 33%
• RNA Binding 33%
• Penetrance 33%
• Exome Sequencing 33%
• POU Domain 33%
• DNA-binding Protein 33%
• Homo sapiens 33%
• Deficiency 33%