Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services - Roberts, Jennifer L.; Hovanes, Karine; Dasouki, Majed; Manzardo, Ann M.; Butler, Merlin G. (Gene, 2014)
Keywords: Adolescent; Adult; autism; Autism spectrum disorders (ASD); Child; Child Development Disorders, Pervasive - genetics; Child, Preschool; Chromosomal microarray analysis; Chromosome Aberrations; chromosomes; Copy number variant (CNV); Developmental delay; Female; females; Genetic Services; genome; Humans; Infant; learning; Learning Disabilities - genetics; Learning disability; Male; males; Microarray Analysis; microarray technology; Middle Aged; oligonucleotides; patients; seizures; Young Adult; YWHAE; PTEN; Developmental delay; PARK2; EEF1B2; ACOXL; ACADL; Learning disability; ZNF407; SACS; POLG; LINS; USP6; EEG; ADIPOQ; COBL; PTH2R; SUMF1; HAX1; MYL1; IL1RAPL1; NDUFS1; SHANK3; HDAC; NLGN2; ANKRD11; CHRNA7; NRXN1; RPE; MRPL19; ITPR1; Chromosomal microarray analysis; XIAP; Autism spectrum disorders (ASD); CNV; FBXO45; CACNA1C; PRPF8; aCGH; FAM117B; KNG1; SD; ASD; BCL2L11; FXR2; ANOVA; MAP2; GALR1; LMNA; NPHP1; SHOX; A2BP1; MBP; PAK2; SH2B1; TRAPPC2; Copy number variant (CNV); BAC; FZD5; IDH1; GATAD2B; SMARCA4; ALS2CR8; CT; KLF7; DLG1; STAG2; DLG4; DNA; FAT1