3982656

Source:http://linkedlifedata.com/resource/pubmed/id/3982656

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004083, umls-concept:C0008625, umls-concept:C0022283
pubmed:issue	4
pubmed:dateCreated	1985-5-8
pubmed:abstractText	We 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.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	0028-3878
pubmed:author	pubmed-author:MillerC ACA, pubmed-author:ParkerW DWDJr
pubmed:issnType	Print
pubmed:volume	35
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	607-10
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:3982656-Chromosome Aberrations, pubmed-meshheading:3982656-Chromosome Disorders, pubmed-meshheading:3982656-Female, pubmed-meshheading:3982656-Humans, pubmed-meshheading:3982656-Infant, pubmed-meshheading:3982656-Melanosis, pubmed-meshheading:3982656-Pigmentation Disorders
pubmed:year	1985
pubmed:articleTitle	Hypomelanosis of Ito: association with a chromosomal abnormality.
pubmed:publicationType	Journal Article, Case Reports