1085923

Source:http://linkedlifedata.com/resource/pubmed/id/1085923

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015306, umls-concept:C2827424
pubmed:issue	2
pubmed:dateCreated	1976-12-1
pubmed:abstractText	2 brothers with possible homozygous multiple cartilaginous exostosis (MCE) are reported. The MCE-PD-(Peripheral Dysostosis) syndrome is discussed. A family (father, daughter and son) with Metachondromatosis is presented, and the tendency to spontaneous remission in this condition is emphasized. A "second thought", when considering the diagnosis of mce, seems worthwhile.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0365332
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	0301-0449
pubmed:author	pubmed-author:GiedionAA, pubmed-author:KesztlerRR, pubmed-author:MuggiascaFF
pubmed:issnType	Print
pubmed:day	20
pubmed:volume	3
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	93-100
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:1085923-Child, pubmed-meshheading:1085923-Child, Preschool, pubmed-meshheading:1085923-Chondroma, pubmed-meshheading:1085923-Exostoses, Multiple Hereditary, pubmed-meshheading:1085923-Female, pubmed-meshheading:1085923-Homozygote, pubmed-meshheading:1085923-Humans, pubmed-meshheading:1085923-Male, pubmed-meshheading:1085923-Pedigree, pubmed-meshheading:1085923-Syndrome
pubmed:year	1975
pubmed:articleTitle	The widened spectrum of multiple cartilaginous exostosis (MCE).
pubmed:publicationType	Journal Article, Case Reports