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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2011-1-6
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pubmed:abstractText |
Germline hSNF5/INI1 mutations are responsible for hereditary cases of rhabdoid tumors (RT) that constitute the rhabdoid predisposition syndrome (RPS). Our study provides the first precise overview of the prevalence of RPS within a large cohort of RT.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1078-0432
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pubmed:author |
pubmed-author:AndréNicolasN,
pubmed-author:AudryGeorgesG,
pubmed-author:BergeronChristopheC,
pubmed-author:BourdeautFranckF,
pubmed-author:BrugièresLaurenceL,
pubmed-author:CapraValeriaV,
pubmed-author:CoupierIsabelleI,
pubmed-author:DelattreOlivierO,
pubmed-author:DozFrançoisF,
pubmed-author:DufourChristelleC,
pubmed-author:EvansD GarethDG,
pubmed-author:Figarella-BrangerDominiqueD,
pubmed-author:FréneauxPaulP,
pubmed-author:Gauthier-VillarsMarionM,
pubmed-author:LequinDelphineD,
pubmed-author:MosseriVéroniqueV,
pubmed-author:OberlinOdileO,
pubmed-author:OrbachDanielD,
pubmed-author:PérelYvesY,
pubmed-author:PierronGaëlleG,
pubmed-author:PinasJoan Carles FerreresJC,
pubmed-author:PugetStéphanieS,
pubmed-author:RanchereDominiqueD,
pubmed-author:ReynaudStéphanieS,
pubmed-author:RiallandXavierX,
pubmed-author:StephanJean-LouisJL
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pubmed:copyrightInfo |
©2011 AACR.
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
17
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
31-8
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pubmed:meshHeading |
pubmed-meshheading:21208904-Child,
pubmed-meshheading:21208904-Child, Preschool,
pubmed-meshheading:21208904-Chromosomal Proteins, Non-Histone,
pubmed-meshheading:21208904-DNA-Binding Proteins,
pubmed-meshheading:21208904-Female,
pubmed-meshheading:21208904-Germ-Line Mutation,
pubmed-meshheading:21208904-Humans,
pubmed-meshheading:21208904-Infant,
pubmed-meshheading:21208904-Infant, Newborn,
pubmed-meshheading:21208904-Male,
pubmed-meshheading:21208904-Pregnancy,
pubmed-meshheading:21208904-Rhabdoid Tumor,
pubmed-meshheading:21208904-Transcription Factors,
pubmed-meshheading:21208904-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
Frequent hSNF5/INI1 germline mutations in patients with rhabdoid tumor.
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pubmed:affiliation |
CHU Nantes, Service d'Hémato-Oncologie Pédiatrique, Nantes, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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