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This contiguous gene syndrome is reminiscent of Okihiro syndrome and emphasizes the importance of array\u2010CGH as a diagnostic tool in atypical syndromic presentations with intrafamilial variability. \u00a9 2013 Wiley Periodicals, Inc.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ajmg.a.36054","type":"journal-article","created":{"date-parts":[[2013,5,25]],"date-time":"2013-05-25T05:46:30Z","timestamp":1369460790000},"page":"1797-1802","source":"Crossref","is-referenced-by-count":13,"title":["Contiguous gene deletion of TBX5 and TBX3 leads to a varible phenotype with combined features of holt\u2010oram and ulnar\u2010mammary syndromes"],"prefix":"10.1002","volume":"161","author":[{"given":"Caroline","family":"Alby","sequence":"first","affiliation":[{"name":"Obstetrics and Gynecology Department H\u00f4pital Necker\u2010Enfant Malades, AP\u2010HP Paris 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