1605250

Source:http://linkedlifedata.com/resource/pubmed/id/1605250

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Subject	Predicate	Object	Context
pubmed-article:1605250	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:1605250	lifeskim:mentions	umls-concept:C0000769	lld:lifeskim
pubmed-article:1605250	lifeskim:mentions	umls-concept:C0015426	lld:lifeskim
pubmed-article:1605250	lifeskim:mentions	umls-concept:C0030797	lld:lifeskim
pubmed-article:1605250	lifeskim:mentions	umls-concept:C1836047	lld:lifeskim
pubmed-article:1605250	lifeskim:mentions	umls-concept:C1855905	lld:lifeskim
pubmed-article:1605250	lifeskim:mentions	umls-concept:C0008924	lld:lifeskim
pubmed-article:1605250	lifeskim:mentions	umls-concept:C0424711	lld:lifeskim
pubmed-article:1605250	lifeskim:mentions	umls-concept:C1970780	lld:lifeskim
pubmed-article:1605250	lifeskim:mentions	umls-concept:C0033377	lld:lifeskim
pubmed-article:1605250	pubmed:issue	3	lld:pubmed
pubmed-article:1605250	pubmed:dateCreated	1992-7-16	lld:pubmed
pubmed-article:1605250	pubmed:abstractText	We describe 2 Brazilian sisters with a combination of clinical signs strongly suggesting a new autosomal recessive MCA/MR syndrome.	lld:pubmed
pubmed-article:1605250	pubmed:language	eng	lld:pubmed
pubmed-article:1605250	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:1605250	pubmed:citationSubset	IM	lld:pubmed
pubmed-article:1605250	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:1605250	pubmed:month	Jun	lld:pubmed
pubmed-article:1605250	pubmed:issn	0148-7299	lld:pubmed
pubmed-article:1605250	pubmed:author	pubmed-author:Richieri-Cost...	lld:pubmed
pubmed-article:1605250	pubmed:author	pubmed-author:Guion-Almeida...	lld:pubmed
pubmed-article:1605250	pubmed:author	pubmed-author:RamosA LAL	lld:pubmed
pubmed-article:1605250	pubmed:issnType	Print	lld:pubmed
pubmed-article:1605250	pubmed:day	1	lld:pubmed
pubmed-article:1605250	pubmed:volume	43	lld:pubmed
pubmed-article:1605250	pubmed:owner	NLM	lld:pubmed
pubmed-article:1605250	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:1605250	pubmed:pagination	565-8	lld:pubmed
pubmed-article:1605250	pubmed:dateRevised	2011-11-17	lld:pubmed
pubmed-article:1605250	pubmed:meshHeading	pubmed-meshheading:1605250-...	lld:pubmed
pubmed-article:1605250	pubmed:meshHeading	pubmed-meshheading:1605250-...	lld:pubmed
pubmed-article:1605250	pubmed:meshHeading	pubmed-meshheading:1605250-...	lld:pubmed
pubmed-article:1605250	pubmed:meshHeading	pubmed-meshheading:1605250-...	lld:pubmed
pubmed-article:1605250	pubmed:meshHeading	pubmed-meshheading:1605250-...	lld:pubmed
pubmed-article:1605250	pubmed:meshHeading	pubmed-meshheading:1605250-...	lld:pubmed
pubmed-article:1605250	pubmed:meshHeading	pubmed-meshheading:1605250-...	lld:pubmed
pubmed-article:1605250	pubmed:meshHeading	pubmed-meshheading:1605250-...	lld:pubmed
pubmed-article:1605250	pubmed:meshHeading	pubmed-meshheading:1605250-...	lld:pubmed
pubmed-article:1605250	pubmed:meshHeading	pubmed-meshheading:1605250-...	lld:pubmed
pubmed-article:1605250	pubmed:meshHeading	pubmed-meshheading:1605250-...	lld:pubmed
pubmed-article:1605250	pubmed:year	1992	lld:pubmed
pubmed-article:1605250	pubmed:articleTitle	Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies.	lld:pubmed
pubmed-article:1605250	pubmed:affiliation	Serviço de Genética Clínica, Hospital de Pesquisa e Reabilitação de Lesões Lábio-Palatais, Universidade de São Paulo, Brazil.	lld:pubmed
pubmed-article:1605250	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:1605250	pubmed:publicationType	Case Reports	lld:pubmed