Keyphrases
Neurodevelopmental Disorders
100%
Deleterious mutations
100%
HnRNP
100%
Gene Family
30%
Meta-analysis
15%
HNRNPU
15%
Proband
15%
Related Disorders
15%
Radial Glial Cells
15%
Clinical Presentation
7%
Exome
7%
Gene Expression Analysis
7%
Gene Expression
7%
Diagnostic Strategy
7%
Molecular Pathogenesis
7%
Rare Variants
7%
Clinical Assessment
7%
Disease-associated
7%
Genome Sequencing
7%
Copy number Variation
7%
Genotype-phenotype Correlation
7%
Genetic Disease
7%
Neurodevelopment
7%
Mutation Analysis
7%
Gene Discovery
7%
Clinical Characterization
7%
Phenotypic Analysis
7%
Indel
7%
Molecular Function
7%
Developing Strategy
7%
Sequencing Studies
7%
Pathogenic mutations
7%
Encoding Gene
7%
Single nucleotide Variant
7%
Clinical Case Reports
7%
International Collaboration
7%
Protein Homology
7%
Rare Phenotype
7%
Phenotypic Characterization
7%
HNRNPH2
7%
Mendelian Genes
7%
HnRNPA1
7%
SYNCRIP
7%
Cerebral Cortex Development
7%
Best Studies
7%
Biochemistry, Genetics and Molecular Biology
Multigene Family
100%
Proband
50%
Ribonucleoprotein
50%
Single-Nucleotide Polymorphism
25%
Gene Expression
25%
Gene Expression Profiling
25%
Sequence Homology
25%
Exome
25%
Genetic Disorder
25%
Indel
25%
Genome Sequencing
25%
Nerve Cell Differentiation
25%
Gene Discovery
25%
Neuroscience
Multigene Family
100%
Heterogeneous Nuclear Ribonucleoprotein
75%
Meta-Analysis
50%
Gene Expression
50%
Expression Analysis
25%
Single-Nucleotide Polymorphism
25%
Nerve Cell Differentiation
25%
Clinical Assessment
25%
Sequence Homology
25%
Indel Mutation
25%