590672

Source:http://linkedlifedata.com/resource/pubmed/id/590672

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0039082, umls-concept:C0314603, umls-concept:C0439659, umls-concept:C1880022
pubmed:issue	7
pubmed:dateCreated	1978-2-18
pubmed:language	spa
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0010333
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	0016-3813
pubmed:author	pubmed-author:ArmendaresSS, pubmed-author:SalamancaFF
pubmed:issnType	Print
pubmed:volume	113
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	321-34
pubmed:dateRevised	2009-11-11
pubmed:meshHeading	pubmed-meshheading:590672-Child, Preschool, pubmed-meshheading:590672-Chromosome Aberrations, pubmed-meshheading:590672-Chromosome Disorders, pubmed-meshheading:590672-Female, pubmed-meshheading:590672-Genetic Diseases, Inborn, pubmed-meshheading:590672-Humans, pubmed-meshheading:590672-Infant, pubmed-meshheading:590672-Infant, Newborn, pubmed-meshheading:590672-Karyotyping, pubmed-meshheading:590672-Male, pubmed-meshheading:590672-Pedigree, pubmed-meshheading:590672-Syndrome
pubmed:year	1977
pubmed:articleTitle	[Characterization of the new syndromes of genetic origin].
pubmed:publicationType	Journal Article, Case Reports