Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects - Zhao, Yingjie; Guo, Tingwei; Fiksinski, Ania; Breetvelt, Elemi; McDonald‐McGinn, Donna M.; Crowley, Terrence B.; Diacou, Alexander; Schneider, Maude; Eliez, Stephan; Swillen, Ann; Breckpot, Jeroen; Vermeesch, Joris; et al. (American journal of medical genetics. Part A, 2018)
Keywords: 22q11.2 deletion syndrome; Adolescent; Adult; Base pairs; Child; Chromosome Deletion; Chromosomes, Human, Pair 22; Coronary artery disease; deletion size; DiGeorge Syndrome - genetics; DiGeorge Syndrome - psychology; Female; Gene deletion; Haploinsufficiency; Heart diseases; Homologous recombination; Humans; intellectual disability; Intellectual Disability - genetics; Intelligence; Intelligence Tests; low copy repeat; Male; Meiosis; segmental duplication; 22q11.2 deletion syndrome; IQ; low copy repeat; segmental duplication; deletion size; intellectual disability