Source:http://linkedlifedata.com/resource/pubmed/id/21508141
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2011-7-7
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pubmed:abstractText |
The Wilms' tumor suppressor gene (WT1) is one of the major regulators of early gonadal and kidney development. WT1 mutations have been identified in 46,XY disorders of sex development (DSD) with associated kidney disease and in few isolated forms of 46,XY DSD.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1945-7197
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
96
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
E1131-6
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pubmed:meshHeading |
pubmed-meshheading:21508141-46, XY Disorders of Sex Development,
pubmed-meshheading:21508141-Adult,
pubmed-meshheading:21508141-Genetic Association Studies,
pubmed-meshheading:21508141-Gonadal Dysgenesis, 46,XY,
pubmed-meshheading:21508141-Humans,
pubmed-meshheading:21508141-Male,
pubmed-meshheading:21508141-Mutation,
pubmed-meshheading:21508141-Phenotype,
pubmed-meshheading:21508141-WT1 Proteins
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pubmed:year |
2011
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pubmed:articleTitle |
Analysis of the Wilms' tumor suppressor gene (WT1) in patients 46,XY disorders of sex development.
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pubmed:affiliation |
Department of Pediatric Endocrinology, University Children's Hospital, Charité, Augustenburger Platz 1, 13353 Berlin, Germany. birgit.koehler@charite.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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