4386913

Source:http://linkedlifedata.com/resource/pubmed/id/4386913

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0021270, umls-concept:C0152021, umls-concept:C0175694
pubmed:issue	6
pubmed:dateCreated	1969-1-3
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0375410
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0022-3476
pubmed:author	pubmed-author:DimichII, pubmed-author:NeedlesC FCF, pubmed-author:ParkS CSC, pubmed-author:SussmanLL
pubmed:issnType	Print
pubmed:volume	73
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	896-902
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:4386913-Abnormalities, Multiple, pubmed-meshheading:4386913-Cryptorchidism, pubmed-meshheading:4386913-Face, pubmed-meshheading:4386913-Fingers, pubmed-meshheading:4386913-Genitalia, Male, pubmed-meshheading:4386913-Growth, pubmed-meshheading:4386913-Heart Defects, Congenital, pubmed-meshheading:4386913-Humans, pubmed-meshheading:4386913-Hypospadias, pubmed-meshheading:4386913-Infant, Newborn, pubmed-meshheading:4386913-Intellectual Disability, pubmed-meshheading:4386913-Male, pubmed-meshheading:4386913-Pedigree, pubmed-meshheading:4386913-Syndactyly, pubmed-meshheading:4386913-Toes
pubmed:year	1968
pubmed:articleTitle	Congenital heart disease in an infant with the Smith-Lemli-Opitz syndrome.
pubmed:publicationType	Journal Article