KnowraFragile X syndromeLinked fromLinked fromThe 5 pages that link to Fragile X syndrome, each with the reason it gives.All 5Broader topic 4Related 1X-linked inheritanceBroader topic: Its X-linked transmission is distinctive, though repeat expansion complicates simple dominant patterns.DNA methylationRelated: Expanded repeats promote FMR1 promoter methylation and gene silencing.X chromosomeBroader topic: FMR1 is on the X chromosome, and repeat expansion alters its expression.Sex-linked inheritanceBroader topic: Its X-linked location combines with unusual repeat expansion and variable effects across sexes.Developmental disabilityBroader topic: It is a genetic cause of intellectual disability and other developmental differences.