Hibridación Genómica Comparativa/métodos; Discapacidad Intelectual/diagnóstico; Discapacidad Intelectual/genética; Adolescente; Niño; Preescolar; Aberraciones Cromosómicas; Cromosomas Humanos Par 11/genética; Cromosomas Humanos Par 4/genética; Estudios de Cohortes; Variaciones en el Número de Copia de ADN/genética; Femenino; Humanos; Masculino; Federación de Rusia

ABLIM3; ACAD10; ADHD; AFAP1L1; AGA; ASTN1; Array comparative genomic hybridization (array CGH); CASP3; CGH; CHERISH; CNS; CNTN6; CNV; Copy number variation (CNV); DDX10; DEAD (Asp-Glu-Ala-Asp) box polypeptide 10; DECIPHER; EEG; EU; European Union; FJX1; GLRA3; HAND2; HFE; ID; IFN; IL17B; ING2; IQ; IRF1; IRF2; Intellectual disability; LDLRAD3; METTL4; MMP14; MMSs; MRI; NDC80; NDC80 kinetochore complex component; NEIL3; NO; OMIM; PCR; PL CNS; PON1; PON2; PON3; SBF; SCGN; SCRG1; SET domain binding factor; SLC1A2; SLC5A7; SLC7A7; SMCHD1; SUFU; SWAP switching B-cell complex 70kDa subunit; SWAP70; Ski-related novel protein N; SnoN; TGFß; TNR; TRIM44; WAGR; Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome; actin binding LIM protein family, member 3; actin filament associated protein 1-like 1; acyl-CoA dehydrogenase family, member 10; aspartylglucosaminidase; astrotactin 1; attention-deficit hyperactivity disorder; caspase 3, apoptosis-related cysteine peptidase; central nervous system; comparative genomic hybridization; contactin 6; copy number variation; database of chromosomal imbalance and phenotype in humans using ensembl resources; electroencephalogram; four jointed box 1 (Drosophila); glycine receptor, alpha 3; grant of European Community's Seventh Framework Programme; heart and neural crest derivatives expressed 2; hemochromatosis; inhibitor of growth family, member 2; intellectual disability; intelligence quotient; interferon; interferon regulatory factor 1; interferon regulatory factor 2; interleukin 17B; low density lipoprotein receptor class A domain containing 3; magnetic resonance imaging; matrix metallopeptidase 14 (membrane-inserted); methyltransferase like 4; microdeletion/microduplication syndromes; nei endonuclease VIII-like 3 (E. coli); nitrogen oxide; online mendelian inheritance in man; paraoxonase 1; paraoxonase 2; paraoxonase 3; perinatal lesion of central nervous system; polymerase chain reaction; qPCR; quantitative PCR; secretagogin, EF-hand calcium binding protein; solute carrier family 1 (glial high affinity glutamate transporter), member 2; solute carrier family 5 (sodium/choline cotransporter), member 7; solute carrier family 7 (amino acid transporter light chain, y+L system), member 7; stimulator of chondrogenesis 1; structural maintenance of chromosomes flexible hinge domain containing 1; suppressor of fused homolog (Drosophila); tenascin R; transforming growth factor beta; tripartite motif containing 44