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Microarray identified a 64.5 KB interstitial deletion of 2q25.3, which includes one exon of <jats:italic>MYT1L<\/jats:italic>. Mutations and deletions in <jats:italic>MTY1L<\/jats:italic> have been associated with autosomal dominant intellectual disability, autistic features, and obesity. Association of these features and 2p25.3 microdeletion has not been reported previously. This case emphasizes the importance of detailed microarray analysis following the sonographic recognition of subtle fetal dysmorphic features.<\/jats:p>","DOI":"10.1002\/jcu.22863","type":"journal-article","created":{"date-parts":[[2020,5,24]],"date-time":"2020-05-24T08:00:22Z","timestamp":1590307222000},"page":"486-488","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Mid\u2010trimester fetal facial dysmorphology associated with 2p25.3 microdeletion"],"prefix":"10.1002","volume":"48","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-1764-8797","authenticated-orcid":false,"given":"David M.","family":"Sherer","sequence":"first","affiliation":[{"name":"The Division of Maternal Fetal Medicine, The Department of Obstetrics and Gynecology State University of New York (SUNY), Downstate Health Sciences University  Brooklyn New York 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