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We present a mother and son who have a 672\u2009kb microdeletion at 1q24q25. They have the typical skeletal features previously described but do not have any associated intellectual disability. We compare the genes within our patients' deletion to those in the deletions of previously reported cases. This indicates two genes that may be implicated in the intellectual disability usually associated with this deletion syndrome; <jats:italic>PIGC<\/jats:italic> and <jats:italic>C1orf105<\/jats:italic>. In addition, our cases provide supporting evidence to recent published work suggesting that the skeletal features may be linked to the microRNAs <jats:italic>miR199<\/jats:italic> and <jats:italic>miR214<\/jats:italic>, encoded within intron 14 of the Dynamin\u20103 gene.<\/jats:p>","DOI":"10.1002\/ajmg.a.40426","type":"journal-article","created":{"date-parts":[[2018,8,7]],"date-time":"2018-08-07T09:29:33Z","timestamp":1533634173000},"page":"2004-2008","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":12,"title":["1q24 deletion syndrome. 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