9829913

Source:http://linkedlifedata.com/resource/pubmed/id/9829913

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0016667, umls-concept:C0021920, umls-concept:C0162735, umls-concept:C0750558, umls-concept:C1414649, umls-concept:C1524003
pubmed:issue	6
pubmed:dateCreated	1999-6-4
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/9829913-9375856
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9215429
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/FMR1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Fragile X Mental Retardation Protein, http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Proteins
pubmed:status	MEDLINE
pubmed:issn	1059-7794
pubmed:author	pubmed-author:GurlingH MHM, pubmed-author:VincentJ BJB
pubmed:issnType	Print
pubmed:volume	12
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	431-2
pubmed:dateRevised	2005-11-17
pubmed:meshHeading	pubmed-meshheading:9829913-Fragile X Mental Retardation Protein, pubmed-meshheading:9829913-Fragile X Syndrome, pubmed-meshheading:9829913-Humans, pubmed-meshheading:9829913-Introns, pubmed-meshheading:9829913-Male, pubmed-meshheading:9829913-Nerve Tissue Proteins, pubmed-meshheading:9829913-Point Mutation, pubmed-meshheading:9829913-RNA-Binding Proteins
pubmed:year	1998
pubmed:articleTitle	Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome.
pubmed:publicationType	Letter, Comment