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The third child had features of both DiGeorge and velo\u2010cardio\u2010facial syndrome (VCFS). The father presented with features compatible with VCFS. This observation further illustrates the wide variability in expression of a submicroscopic deletion of 22q11, even within one family.<\/jats:p>","DOI":"10.1111\/j.1399-0004.1997.tb02463.x","type":"journal-article","created":{"date-parts":[[2010,7,19]],"date-time":"2010-07-19T10:14:25Z","timestamp":1279534465000},"page":"246-249","source":"Crossref","is-referenced-by-count":12,"title":["Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father Clinical variability of 22q11 deletion"],"prefix":"10.1111","volume":"51","author":[{"given":"K.","family":"Devriendt","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R. Van","family":"Hoestenberghe","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C. 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