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pubmed-article:3982656pubmed:abstractTextWe report the clinical and neuroradiologic findings and the association of a chromosome abnormality, t(2,8), with a case of hypomelanosis of Ito (incontinentia pigmenti achromians). Chromosome anomalies have not been previously recognized in this genetically determined, neurocutaneous disorder.lld:pubmed
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pubmed-article:3982656pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:3982656pubmed:articleTitleHypomelanosis of Ito: association with a chromosomal abnormality.lld:pubmed
pubmed-article:3982656pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3982656pubmed:publicationTypeCase Reportslld:pubmed
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