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Mutation analysis of <jats:italic>EYA1<\/jats:italic>, <jats:italic>SIX1<\/jats:italic>, and <jats:italic>SIX5<\/jats:italic>, genes that underlie otofaciocervical and\/or branchio\u2010oto\u2010renal syndrome, was negative. Pathologic diagnosis of the excised cervical sinus tracts was revised on re\u2010examination to heterotopic salivary gland tissue. Using high resolution chromosomal microarray analysis, we identified a novel 2.52 Mb deletion at 19p13.12, which was confirmed by fluorescent in situ hybridization and demonstrated to be a de novo mutation by testing of the parents. Overall, deletions of chromosome 19p13 are rare. \u00a9 2009 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.32691","type":"journal-article","created":{"date-parts":[[2009,2,12]],"date-time":"2009-02-12T23:58:00Z","timestamp":1234483080000},"page":"396-402","source":"Crossref","is-referenced-by-count":30,"title":["A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies"],"prefix":"10.1002","volume":"149A","author":[{"given":"Daniel R.","family":"Jensen","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Donna M.","family":"Martin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Stephen","family":"Gebarski","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Trilochan","family":"Sahoo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ellen K.","family":"Brundage","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A. 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