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pubmed-article:10951468pubmed:abstractTextAcampomelic campomelic dysplasia is a rare clinical variant of the more commonly encountered campomelic dysplasia (CMD1), characterized by absence of long bone curvature (acampomelia). We present a patient with acampomelic CMD1 with a de novo SOX9 missense mutation and report his clinical course to age one year, thereby contributing to genotype-phenotype correlation in CMD1. 2000.lld:pubmed
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pubmed-article:10951468pubmed:authorpubmed-author:ThongM KMKlld:pubmed
pubmed-article:10951468pubmed:copyrightInfoCopyright 2000 Wiley-Liss, Inc.lld:pubmed
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pubmed-article:10951468pubmed:pagination421-5lld:pubmed
pubmed-article:10951468pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:10951468pubmed:articleTitleAcampomelic campomelic dysplasia with SOX9 mutation.lld:pubmed
pubmed-article:10951468pubmed:affiliationSouth Australian Clinical Genetics Service, Women's and Children's Hospital, North Adelaide, South Australia, Australia. thongm@cryptic.rch.unimelb.edu.aulld:pubmed
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