Keyphrases
Readability
100%
Dyslexia
100%
Normal Reading
100%
Periventricular Nodular Heterotopia
100%
Filamin A mutation
100%
Filamin A
40%
Evidence Support
20%
Behavioral Outcomes
20%
Cognitive Profile
20%
Inheritance Pattern
20%
Variable Groups
20%
Neuroimaging
20%
Genetic Causes
20%
Gene Expression Pattern
20%
Novel mutation
20%
Neuronal Migration
20%
X Chromosome Inactivation
20%
Genetic Factors
20%
Nodule
20%
Genetic Disease
20%
Clinical Practice
20%
Fetal Development
20%
Heterogeneous Disorder
20%
Normal Intelligence
20%
Seizure Disorder
20%
Multiple Lines of Evidence
20%
Reading Profiles
20%
X-linked Inheritance
20%
Heterotopia
20%
Gray Matter Heterotopia
20%
Specific Reading
20%
Reading Fluency
20%
Mother-daughter Pairs
20%
Medicine and Dentistry
Dyslexia
100%
Literacy
100%
Periventricular Heterotopia
100%
Filamin A
100%
Disease
60%
Heterotopia
40%
Epileptic Seizure
20%
Morphology
20%
Genetic Disorder
20%
Heredity
20%
Anatomy
20%
Fetus Development
20%
Dominant Inheritance
20%
Gray Matter
20%
X Chromosome Inactivation
20%
Neuroscience
Dyslexia
100%
Filamin A
100%
Gray Matter
33%
Neuronal Migration
33%
Epilepsy
33%
X Chromosome Inactivation
33%