16303781

Source:http://linkedlifedata.com/resource/pubmed/id/16303781

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0205314, umls-concept:C0235946, umls-concept:C0449450, umls-concept:C0599155, umls-concept:C0679622, umls-concept:C0694898, umls-concept:C0950121
pubmed:issue	2
pubmed:dateCreated	2006-1-19
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8706402
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/WT1 Proteins
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0931-0509
pubmed:author	pubmed-author:DrechslerMatthiasM, pubmed-author:EssayieMaximillianM, pubmed-author:MüllerDominikD, pubmed-author:QuerfeldUweU, pubmed-author:Royer-PokoraBrigitteB, pubmed-author:SchumacherValérieV, pubmed-author:ThumfartJuliaJ
pubmed:issnType	Print
pubmed:volume	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	518-21
pubmed:meshHeading	pubmed-meshheading:16303781-Atrophy, pubmed-meshheading:16303781-Child, Preschool, pubmed-meshheading:16303781-Corpus Callosum, pubmed-meshheading:16303781-Denys-Drash Syndrome, pubmed-meshheading:16303781-Follow-Up Studies, pubmed-meshheading:16303781-Humans, pubmed-meshheading:16303781-Infant, pubmed-meshheading:16303781-Karyotyping, pubmed-meshheading:16303781-Male, pubmed-meshheading:16303781-Mutation, Missense, pubmed-meshheading:16303781-WT1 Proteins
pubmed:year	2006
pubmed:articleTitle	A novel WT1 missense mutation presenting with Denys-Drash syndrome and cortical atrophy.
pubmed:affiliation	Institute of Human Genetics, Heinrich-Heine University Düsseldorf , Germany.
pubmed:publicationType	Journal Article, Case Reports