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pubmed-article:12239727pubmed:abstractTextMany types of chromosome mosaicism have been identified in cases of hypomelanosis of Ito, often in association with chromosome instability; however, there have been very few cases with diploid-tetraploid mosaicism described in the literature. We present a patient with a tetraploid mosaicism: a 17-year-old girl who has hypomelanosis of Ito in association with diploid/tetraploid/t(1;6) mosaicism. She had multiple congenital anomalies of omphalocele, exstrophy of bladder, duodenal web, and imperforate anus. These features have not been described previously in diploid-tetraploid mosaicism.lld:pubmed
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pubmed-article:12239727pubmed:authorpubmed-author:LeonardN JNJlld:pubmed
pubmed-article:12239727pubmed:authorpubmed-author:TomkinsD JDJlld:pubmed
pubmed-article:12239727pubmed:copyrightInfoCopyright 2002 Wiley-Liss, Inc.lld:pubmed
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pubmed-article:12239727pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:12239727pubmed:articleTitleDiploid/tetraploid/t(1;6) mosaicism in a 17-year-old female with hypomelanosis of Ito, multiple congenital anomalies, and body asymmetry.lld:pubmed
pubmed-article:12239727pubmed:affiliationEdmonton Genetics Clinic, Department of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada. nleonard@cha.ab.calld:pubmed
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