{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,16]],"date-time":"2026-10-16T16:09:09Z","timestamp":1792166949072,"version":"4.4.0"},"reference-count":19,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2008,4,30]],"date-time":"2008-04-30T00:00:00Z","timestamp":1209513600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2008,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Interstitial deletions involving the chromosomal band 15q15 are very rare. A total of five cases were previously reported. Here another case of a 15q15.2\u2010q22.2 deletion is reported, presenting with severe craniosynostosis of coronary, metopic, and sagittal sutures. The chromosome 15 with the 17.7\u2010Mb deletion was of the paternal origin. A critical region for craniosynostosis may be located at the 734\u2010kb segment at 15q15.2. Interestingly, the entire <jats:italic>FBN1<\/jats:italic> gene was deleted in this patient. \u00a9 2008 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.32339","type":"journal-article","created":{"date-parts":[[2008,4,30]],"date-time":"2008-04-30T20:17:07Z","timestamp":1209586627000},"page":"1462-1465","source":"Crossref","is-referenced-by-count":20,"title":["Craniosynostosis in a patient with a de novo 15q15\u2010q22 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