12389203

Source:http://linkedlifedata.com/resource/pubmed/id/12389203

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007320, umls-concept:C0085973, umls-concept:C0265202
pubmed:issue	1
pubmed:dateCreated	2002-10-21
pubmed:language	spa
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7706841
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0210-0010
pubmed:author	pubmed-author:Infante-VelásquezE JEJ, pubmed-author:OrtegaM AMA, pubmed-author:Pérez del CampoY HYH
pubmed:issnType	Print
pubmed:volume	35
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	99-100
pubmed:dateRevised	2009-5-28
pubmed:meshHeading	pubmed-meshheading:12389203-Abnormalities, Multiple, pubmed-meshheading:12389203-Adolescent, pubmed-meshheading:12389203-Chromosomes, Human, Pair 3, pubmed-meshheading:12389203-Dwarfism, pubmed-meshheading:12389203-Fetal Growth Retardation, pubmed-meshheading:12389203-Humans, pubmed-meshheading:12389203-Male, pubmed-meshheading:12389203-Syndrome
pubmed:articleTitle	[Seckel syndrome: a case report].
pubmed:affiliation	Centro Internacional de Restauración Neurológica (CIREN), La Habana, Cuba. erduy@neuro.sld.cu
pubmed:publicationType	Journal Article, Case Reports