Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial casesMelita Irving, Jonathan Berg, Angela Davies et al.|American Journal of Medical Genetics Part A|2003Cited by 68
Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort studyShelagh Joss, Francesca Wicks, Ramya Srinivasan et al.|The Lancet Psychiatry|2022Cited by 52
De novo and biallelic DEAF1 variants cause a phenotypic spectrumMaria João Nabais Sá, Anneke T. Vulto-vanSilfhout, Philip J. Jensik et al.|Genetics in Medicine|2019Cited by 33