11370628

Source:http://linkedlifedata.com/resource/pubmed/id/11370628

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Subject	Predicate	Object	Context
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pubmed-article:11370628	pubmed:issue	4	lld:pubmed
pubmed-article:11370628	pubmed:dateCreated	2001-5-22	lld:pubmed
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pubmed-article:11370628	pubmed:status	MEDLINE	lld:pubmed
pubmed-article:11370628	pubmed:month	Apr	lld:pubmed
pubmed-article:11370628	pubmed:issn	1468-6244	lld:pubmed
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pubmed-article:11370628	pubmed:issnType	Electronic	lld:pubmed
pubmed-article:11370628	pubmed:volume	38	lld:pubmed
pubmed-article:11370628	pubmed:owner	NLM	lld:pubmed
pubmed-article:11370628	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:11370628	pubmed:pagination	244-9	lld:pubmed
pubmed-article:11370628	pubmed:dateRevised	2008-11-21	lld:pubmed
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pubmed-article:11370628	pubmed:year	2001	lld:pubmed
pubmed-article:11370628	pubmed:articleTitle	Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus.	lld:pubmed
pubmed-article:11370628	pubmed:publicationType	Letter	lld:pubmed
pubmed-article:11370628	pubmed:publicationType	Research Support, U.S. Gov't, P.H.S.	lld:pubmed
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