Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH - Tyson, C.; Harvard, C.; Locker, R.; Friedman, J.M.; Langlois, S.; Lewis, M.E.S.; Van Allen, M.; Somerville, M.; Arbour, L.; Clarke, L.; McGilivray, B.; Yong, S.L.; et al. (American journal of medical genetics. Part A, 2005)
Keywords: 11q12.3-13.1; 7q36.3; array CGH; Chromosome Aberrations; Chromosome Disorders - genetics; Chromosomes, Human, Pair 11 - genetics; Chromosomes, Human, Pair 7 - genetics; Chromosomes, Human, X - genetics; de novo microdeletion and microduplication; DNA Primers; Female; Humans; In Situ Hybridization, Fluorescence; intellectual disability; Intellectual Disability - genetics; Male; Microsatellite Repeats - genetics; Nucleic Acid Hybridization - genetics; Oligonucleotide Array Sequence Analysis - methods; Pedigree; Polymerase Chain Reaction; Xp22.3