17639592

Source:http://linkedlifedata.com/resource/pubmed/id/17639592

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0028326
pubmed:issue	3
pubmed:dateCreated	2007-8-2
pubmed:abstractText	Noonan syndrome is a common autosomal dominant condition caused by multiple genes in the RasMAPK pathway. The adult phenotype can be extremely subtle, and many adults are diagnosed only after the birth of a more obviously affected child. Whether diagnosis is made in childhood or adulthood, initial and ongoing evaluation of many systems can have considerable health benefits.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235745
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	1552-4868
pubmed:author	pubmed-author:AllansonJudith EJE
pubmed:copyrightInfo	(c) 2007 Wiley-Liss, Inc.
pubmed:issnType	Print
pubmed:day	15
pubmed:volume	145C
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	274-9
pubmed:dateRevised	2008-5-21
pubmed:meshHeading	pubmed-meshheading:17639592-Facies, pubmed-meshheading:17639592-Humans, pubmed-meshheading:17639592-Noonan Syndrome
pubmed:year	2007
pubmed:articleTitle	Noonan syndrome.
pubmed:affiliation	Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada. allanson@cheo.on.ca
pubmed:publicationType	Journal Article, Review