9463338

Source:http://linkedlifedata.com/resource/pubmed/id/9463338

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Predicate	Object
rdf:type	pubmed:Citation
pubmed:issue	2
pubmed:dateCreated	1998-4-6
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370475
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome b Group, http://linkedlifedata.com/resource/pubmed/chemical/DNA, Mitochondrial
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0002-9297
pubmed:author	pubmed-author:BarrattTT, pubmed-author:BolhuisPP, pubmed-author:ChanCC, pubmed-author:HückelWW, pubmed-author:HowellNN, pubmed-author:NikoskelainenEE, pubmed-author:NorbySS, pubmed-author:OostraR JRJ, pubmed-author:PoultonJJ, pubmed-author:RosenbergTT, pubmed-author:SavontausM LML
pubmed:issnType	Print
pubmed:volume	62
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	492-5
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:9463338-Cytochrome b Group, pubmed-meshheading:9463338-DNA, Mitochondrial, pubmed-meshheading:9463338-Female, pubmed-meshheading:9463338-Genomic Imprinting, pubmed-meshheading:9463338-Humans, pubmed-meshheading:9463338-Male, pubmed-meshheading:9463338-Optic Atrophies, Hereditary, pubmed-meshheading:9463338-Pedigree, pubmed-meshheading:9463338-Point Mutation
pubmed:year	1998
pubmed:articleTitle	Reply to Hofmann et al.
pubmed:publicationType	Letter