1388933

Source:http://linkedlifedata.com/resource/pubmed/id/1388933

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0018784, umls-concept:C0022283, umls-concept:C0205082
pubmed:issue	3
pubmed:dateCreated	1992-11-25
pubmed:abstractText	In this report we describe an 8-year-old boy of Algerian origin with profound sensorineural deafness and skin pigmentation anomalies consistent with the diagnosis of hypomelanosis of Ito. On the basis of this observation the etiologic heterogeneity of this condition is discussed.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9015261
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	1015-8146
pubmed:author	pubmed-author:DereymaekerA MAM, pubmed-author:FrynsJ PJP, pubmed-author:Van Den BergheHH
pubmed:issnType	Print
pubmed:volume	3
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	149-51
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:1388933-Abnormalities, Multiple, pubmed-meshheading:1388933-Child, pubmed-meshheading:1388933-Deafness, pubmed-meshheading:1388933-Humans, pubmed-meshheading:1388933-Intellectual Disability, pubmed-meshheading:1388933-Male, pubmed-meshheading:1388933-Mutation, pubmed-meshheading:1388933-Pigmentation Disorders, pubmed-meshheading:1388933-Syndrome
pubmed:year	1992
pubmed:articleTitle	Hypomelanosis of Ito and severe sensorineural deafness.
pubmed:affiliation	Centre for Human Genetics, University of Leuven, Belgium.
pubmed:publicationType	Journal Article, Case Reports