Activity-dependent mRNA translation at synapses to spine remodeling: insights into mental retardation.
A genomic approach for the identification of genes involved in mental retardation and brain anomalies.
Hyperconnectivity and slow synapses during early development of medial prefrontal cortex in a mouse model for mental retardation and autism
Molecular karyotyping: a powerful tool for the study of genomic defects in patients with mental retardation
Multiple Genomic Aberrations in a Patient With Mental Retardation and Hypogonadism: 45,X/46,X,psu dic(Y) Karyotype, Thyroid Hormone Receptor Beta (THRB) Mutation and Heterozygosity for Wilson Disease
Autosomal dominant syndrome of mental retardation, hypotelorism, and cleft palate resembling Schilbach-Rott syndrome