3308683

Source:http://linkedlifedata.com/resource/pubmed/id/3308683

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Subject	Predicate	Object	Context
pubmed-article:3308683	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:3308683	lifeskim:mentions	umls-concept:C0080178	lld:lifeskim
pubmed-article:3308683	lifeskim:mentions	umls-concept:C0000769	lld:lifeskim
pubmed-article:3308683	lifeskim:mentions	umls-concept:C1848873	lld:lifeskim
pubmed-article:3308683	lifeskim:mentions	umls-concept:C1968945	lld:lifeskim
pubmed-article:3308683	lifeskim:mentions	umls-concept:C1524119	lld:lifeskim
pubmed-article:3308683	lifeskim:mentions	umls-concept:C0039082	lld:lifeskim
pubmed-article:3308683	lifeskim:mentions	umls-concept:C0443147	lld:lifeskim
pubmed-article:3308683	pubmed:issue	2	lld:pubmed
pubmed-article:3308683	pubmed:dateCreated	1987-11-17	lld:pubmed
pubmed-article:3308683	pubmed:abstractText	Three members of a nuclear family were affected by split hands and feet or syndactyly, obstructive urinary anomalies and spina bifida or diaphragmatic defect.	lld:pubmed
pubmed-article:3308683	pubmed:language	eng	lld:pubmed
pubmed-article:3308683	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:3308683	pubmed:citationSubset	IM	lld:pubmed
pubmed-article:3308683	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:3308683	pubmed:month	Oct	lld:pubmed
pubmed-article:3308683	pubmed:issn	0340-6717	lld:pubmed
pubmed-article:3308683	pubmed:author	pubmed-author:CzeizelAA	lld:pubmed
pubmed-article:3308683	pubmed:author	pubmed-author:LosonciAA	lld:pubmed
pubmed-article:3308683	pubmed:issnType	Print	lld:pubmed
pubmed-article:3308683	pubmed:volume	77	lld:pubmed
pubmed-article:3308683	pubmed:owner	NLM	lld:pubmed
pubmed-article:3308683	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:3308683	pubmed:pagination	203-4	lld:pubmed
pubmed-article:3308683	pubmed:dateRevised	2004-11-17	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:meshHeading	pubmed-meshheading:3308683-...	lld:pubmed
pubmed-article:3308683	pubmed:year	1987	lld:pubmed
pubmed-article:3308683	pubmed:articleTitle	Split hand, obstructive urinary anomalies and spina bifida or diaphragmatic defect syndrome with autosomal dominant inheritance.	lld:pubmed
pubmed-article:3308683	pubmed:affiliation	Department of Human Genetics and Teratology, WHO Collaborating Centre for the Community Control of Hereditary Diseases, Budapest, Hungary.	lld:pubmed
pubmed-article:3308683	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:3308683	pubmed:publicationType	Case Reports	lld:pubmed