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Since one locus for Opitz syndrome maps to 22q11.2 and chromosomal arrangements are frequently complex and could inactivate such a locus, we performed high\u2010resolution array\u2010based comparative genomic hybridization (CGH) on a new Opitz syndrome\u2010like phenotype patient with a 22q11.2 deletion. He shares the same deletion as patients with velocardiofacial and DiGeorge syndrome. \u00a9 2007 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.32025","type":"journal-article","created":{"date-parts":[[2007,11,14]],"date-time":"2007-11-14T02:16:37Z","timestamp":1195006597000},"page":"3302-3308","source":"Crossref","is-referenced-by-count":7,"title":["A patient with 22q11.2 deletion and Opitz syndrome\u2010like phenotype has the same deletion as velocardiofacial patients"],"prefix":"10.1002","volume":"143A","author":[{"given":"Robert P.","family":"Erickson","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Teresita D\u00edaz","family":"de St\u00e5hl","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Carl E.G.","family":"Bruder","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jan 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