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pubmed-article:16355815pubmed:abstractTextA 14 year-old girl was found to have a deletion of the distal segment of chromosome 3 [46,XX,Del(3)(q28-29)]. The main features of this presentation were mild intellectual disability, facial dysmorphism, short stature, kypho-scoliosis, and primary ovarian failure, an association that has not been described before in association with chromosome 3 deletion. The phenotype and presentation are compared with those of previous case reports.lld:pubmed
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pubmed-article:16355815pubmed:authorpubmed-author:ZacharinMarga...lld:pubmed
pubmed-article:16355815pubmed:authorpubmed-author:McDonnellCiar...lld:pubmed
pubmed-article:16355815pubmed:authorpubmed-author:NguyenThiThuy...lld:pubmed
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pubmed-article:16355815pubmed:dateRevised2010-11-18lld:pubmed
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pubmed-article:16355815pubmed:year2005lld:pubmed
pubmed-article:16355815pubmed:articleTitlePrimary ovarian failure and deletions of the long arm of chromosome 3.lld:pubmed
pubmed-article:16355815pubmed:affiliationDepartment ofPaediatrics, University of Melbourne, Australia.lld:pubmed
pubmed-article:16355815pubmed:publicationTypeJournal Articlelld:pubmed
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