{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T17:38:04Z","timestamp":1790876284825,"version":"4.1.0"},"reference-count":26,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2010,8,3]],"date-time":"2010-08-03T00:00:00Z","timestamp":1280793600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2010,9]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Array comparative genomic hybridization has increasingly become the standard of care to evaluate patients for genomic imbalance. As the patient population evaluated by microarray expands, there is certain to be an increase in the detection of unexpected, yet common diseases. When array results predict a late\u2010onset disorder or cancer predisposition, it becomes a challenge for physicians and counselors to adequately address with patients. Included in this study were three patients described with nonspecific phenotypic findings who underwent microarray testing to better define their disease etiology. An unexpected deletion within the dystrophin gene was observed in each case, despite that no patient was suspected of a dystrophinopathy at the time of testing. The patients included an 8\u2010day\u2010old male with a dystrophin deletion predictive of Becker muscular dystrophy, an 18\u2010month old female found to be the carrier of deletion, and a 4\u2010year\u20108\u2010month\u2010old male with a deletion predictive of Duchenne muscular dystrophy. In this circumstance it becomes difficult to counsel the family, as well as to predict disease course when underlying medical conditions may exist. However, early detection may enable the patient to receive proactive treatment, and allows for screening of at\u2010risk family members. Ultimately, it is up to the clinician to promote informed decision\u2010making within the family prior to testing, and ensure that adequate counseling is provided during follow\u2010up. \u00a9 2010 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.33532","type":"journal-article","created":{"date-parts":[[2010,8,3]],"date-time":"2010-08-03T22:03:06Z","timestamp":1280872986000},"page":"2301-2307","source":"Crossref","is-referenced-by-count":12,"title":["Unexpected detection of dystrophin gene deletions by array comparative genomic hybridization"],"prefix":"10.1002","volume":"152A","author":[{"given":"Catherine E.","family":"Cottrell","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thomas 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