1866502

Source:http://linkedlifedata.com/resource/pubmed/id/1866502

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0205082, umls-concept:C0410538, umls-concept:C0449450, umls-concept:C1533148
pubmed:issue	1
pubmed:dateCreated	1991-9-10
pubmed:abstractText	A male child who has the clinic and radiologic characteristics of type IV pseudoachondroplasia an autosomal recessive inherited disease, is described. For genetic counselling purposes, the clinic features and differential diagnosis and its classification are discussed.
pubmed:language	spa
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9421552
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0034-8376
pubmed:author	pubmed-author:ManzanoCC, pubmed-author:Quiroz GómezEE, pubmed-author:SalamancaFF, pubmed-author:Silvera-RedondoC ACA
pubmed:issnType	Print
pubmed:volume	43
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	77-9
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:1866502-Achondroplasia, pubmed-meshheading:1866502-Child, pubmed-meshheading:1866502-Humans, pubmed-meshheading:1866502-Male, pubmed-meshheading:1866502-Phenotype, pubmed-meshheading:1866502-Severity of Illness Index
pubmed:articleTitle	[Severe pseudoachondroplasia. Presentation of a case].
pubmed:affiliation	Sección de Genética Hospital de Gineco-Obstetricia No.4 Luis Castelazo Ayala, IMSS, México, D.F.
pubmed:publicationType	Journal Article, English Abstract, Case Reports