16281384

Source:http://linkedlifedata.com/resource/pubmed/id/16281384

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0431399, umls-concept:C0868928, umls-concept:C0936012, umls-concept:C1547011, umls-concept:C1879746
pubmed:issue	10
pubmed:dateCreated	2005-11-11
pubmed:language	rus
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9712194
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	1997-7298
pubmed:author	pubmed-author:AlikhanovA AAA, pubmed-author:GeneralovV OVO, pubmed-author:Il'inaE SES, pubmed-author:MukhinK IuKIu
pubmed:issnType	Print
pubmed:volume	105
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	59-61
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:16281384-Abnormalities, Multiple, pubmed-meshheading:16281384-Apgar Score, pubmed-meshheading:16281384-Brain, pubmed-meshheading:16281384-Cerebellar Ataxia, pubmed-meshheading:16281384-Cerebellum, pubmed-meshheading:16281384-Child, pubmed-meshheading:16281384-Diagnosis, Differential, pubmed-meshheading:16281384-Humans, pubmed-meshheading:16281384-Infant, pubmed-meshheading:16281384-Intellectual Disability, pubmed-meshheading:16281384-Magnetic Resonance Imaging, pubmed-meshheading:16281384-Male, pubmed-meshheading:16281384-Muscle Hypotonia, pubmed-meshheading:16281384-Ocular Motility Disorders, pubmed-meshheading:16281384-Phenotype, pubmed-meshheading:16281384-Polymorphism, Genetic, pubmed-meshheading:16281384-Respiration Disorders, pubmed-meshheading:16281384-Syndrome, pubmed-meshheading:16281384-Tomography, X-Ray Computed
pubmed:year	2005
pubmed:articleTitle	[Neuroradiological aspects of Joubert syndrome: an analysis of two cases].
pubmed:publicationType	Journal Article, Case Reports