20209845

Source:http://linkedlifedata.com/resource/pubmed/id/20209845

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0162359, umls-concept:C0868928
pubmed:issue	12
pubmed:dateCreated	2010-3-8
pubmed:abstractText	Ectodermal dysplasias are rare hereditary diseases characterised by congenital absence of ectodermally derived structures and classified according to four symptoms: trichodysplasia, hypodontia, onychodysplasia and hypohidrosis.
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0413766
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0041-4131
pubmed:author	pubmed-author:BouzgarrouAliaA, pubmed-author:Ezzine SebaiNadiaN, pubmed-author:FazaaBécimaB, pubmed-author:JonesMeriemM, pubmed-author:KamounMohamed RidhaMR, pubmed-author:KhaledAidaA, pubmed-author:KharfiMoniaM, pubmed-author:M'hallaHanaH
pubmed:issnType	Print
pubmed:volume	87
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	805-9
pubmed:meshHeading	pubmed-meshheading:20209845-Abnormalities, Multiple, pubmed-meshheading:20209845-Adolescent, pubmed-meshheading:20209845-Adult, pubmed-meshheading:20209845-Child, pubmed-meshheading:20209845-Child, Preschool, pubmed-meshheading:20209845-Consanguinity, pubmed-meshheading:20209845-Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive, pubmed-meshheading:20209845-Female, pubmed-meshheading:20209845-Humans, pubmed-meshheading:20209845-Infant, pubmed-meshheading:20209845-Male, pubmed-meshheading:20209845-Retrospective Studies, pubmed-meshheading:20209845-Young Adult
pubmed:year	2009
pubmed:articleTitle	[Anhidrotic/hypohidrotic ectodermal dysplasia: ten cases].
pubmed:affiliation	Service Dermatologie, Hôpital Charles Nicolle, Tunis, Tunisie.
pubmed:publicationType	Journal Article, English Abstract