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Although these symptoms have been attributed to deletions of 1q42\u20101q44, the minimal chromosomal region involved has not been identified. Using microsatellite and single nucleotide polymorphism (SNP) markers, we have mapped the deleted regions in seven patients with terminal deletions of chromosome 1q to define a 2.0\u2010Mb microcephaly critical region including the 1q43\u20101q44 boundary and no more than 11 genes. \u00a9 2007 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.31776","type":"journal-article","created":{"date-parts":[[2007,6,29]],"date-time":"2007-06-29T20:47:41Z","timestamp":1183150061000},"page":"1692-1698","source":"Crossref","is-referenced-by-count":59,"title":["A 2\u2010Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome"],"prefix":"10.1002","volume":"143A","author":[{"given":"Anthony D.","family":"Hill","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bernard S.","family":"Chang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R. 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