16416771

Source:http://linkedlifedata.com/resource/pubmed/id/16416771

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012634, umls-concept:C0017337, umls-concept:C0205171
pubmed:dateCreated	2006-1-18
pubmed:language	jpn
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0420546
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0047-1852
pubmed:author	pubmed-author:KurahashiHirokiH, pubmed-author:TaniguchiMarikoM
pubmed:issnType	Print
pubmed:volume	63 Suppl 12
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	57-63
pubmed:dateRevised	2011-7-27
pubmed:meshHeading	pubmed-meshheading:16416771-Female, pubmed-meshheading:16416771-Genes, Dominant, pubmed-meshheading:16416771-Genes, Recessive, pubmed-meshheading:16416771-Genes, X-Linked, pubmed-meshheading:16416771-Genetic Diseases, Inborn, pubmed-meshheading:16416771-Humans, pubmed-meshheading:16416771-Male, pubmed-meshheading:16416771-Pedigree
pubmed:year	2005
pubmed:articleTitle	[Single gene disorder].
pubmed:affiliation	Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University.
pubmed:publicationType	Journal Article, Review