1298036

Source:http://linkedlifedata.com/resource/pubmed/id/1298036

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017398, umls-concept:C0017402
pubmed:issue	4
pubmed:dateCreated	1993-5-4
pubmed:language	spa
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0123071
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, Mitochondrial
pubmed:status	MEDLINE
pubmed:issn	0556-6177
pubmed:author	pubmed-author:BuenoMM, pubmed-author:Pérez-GonzálezJ MJM
pubmed:issnType	Print
pubmed:volume	37
pubmed:geneSymbol	CFTR, FMR-1
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	181-9
pubmed:dateRevised	2009-11-11
pubmed:meshHeading	pubmed-meshheading:1298036-Algorithms, pubmed-meshheading:1298036-Chromosome Aberrations, pubmed-meshheading:1298036-Chromosome Disorders, pubmed-meshheading:1298036-Cystic Fibrosis, pubmed-meshheading:1298036-DNA, Mitochondrial, pubmed-meshheading:1298036-DNA Mutational Analysis, pubmed-meshheading:1298036-Female, pubmed-meshheading:1298036-Fragile X Syndrome, pubmed-meshheading:1298036-Gene Therapy, pubmed-meshheading:1298036-Genetics, Medical, pubmed-meshheading:1298036-Genome, Human, pubmed-meshheading:1298036-Humans, pubmed-meshheading:1298036-Incidence, pubmed-meshheading:1298036-Male, pubmed-meshheading:1298036-Muscular Dystrophies, pubmed-meshheading:1298036-Myotonic Dystrophy, pubmed-meshheading:1298036-Polymerase Chain Reaction, pubmed-meshheading:1298036-Prevalence, pubmed-meshheading:1298036-Spinal Muscular Atrophies of Childhood
pubmed:articleTitle	[Perspectives in medical genetics: the new genetics].
pubmed:affiliation	Departamento de Pediatría, Radiología y Medicina Física, Facultad de Medicina, Universidad de Zaragoza.
pubmed:publicationType	Journal Article, Review