3587189

Source:http://linkedlifedata.com/resource/pubmed/id/3587189

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0265224, umls-concept:C0332148, umls-concept:C0678257, umls-concept:C0678944, umls-concept:C0868928
pubmed:issue	3-4
pubmed:dateCreated	1987-6-29
pubmed:language	ita
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0400740
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0026-4946
pubmed:author	pubmed-author:BelliniCC, pubmed-author:BonioliEE, pubmed-author:GemmeGG, pubmed-author:LagorioVV, pubmed-author:RuffaGG
pubmed:issnType	Print
pubmed:day	28
pubmed:volume	39
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	123-7
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:3587189-Abnormalities, Multiple, pubmed-meshheading:3587189-Facial Expression, pubmed-meshheading:3587189-Humans, pubmed-meshheading:3587189-Infant, Newborn, pubmed-meshheading:3587189-Male, pubmed-meshheading:3587189-Orofaciodigital Syndromes, pubmed-meshheading:3587189-Phenotype
pubmed:year	1987
pubmed:articleTitle	[Freeman-Sheldon syndrome. Description of 2 cases of probable recessive autosomal inheritance].
pubmed:publicationType	Journal Article, English Abstract, Case Reports