Mostrar el registro sencillo del ítem

Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk

dc.contributor.authorCarracedo Álvarez, Ángel
dc.date.accessioned2017-06-07T07:25:02Z
dc.date.available2017-06-07T07:25:02Z
dc.date.issued2015
dc.identifier.issn0964-6906
dc.identifier.urihttp://hdl.handle.net/20.500.11940/6185
dc.language.isoeng
dc.titleFine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk
dc.typeArtigoes
dc.authorsophosJ.N., Painter
dc.authorsophosT.A., O'Mara
dc.authorsophosJ., Batra
dc.authorsophosT., Cheng
dc.authorsophosF.A., Lose
dc.authorsophosJ., Dennis
dc.authorsophosK., Michailidou
dc.authorsophosJ.P., Tyrer
dc.authorsophosS., Ahmed
dc.authorsophosK., Ferguson
dc.authorsophosC.S., Healey
dc.authorsophosS., Kaufmann
dc.authorsophosK.M., Hillman
dc.authorsophosC., Walpole
dc.authorsophosL., Moya
dc.authorsophosP., Pollock
dc.authorsophosA., Jones
dc.authorsophosK., Howarth
dc.authorsophosL., Martin
dc.authorsophosM., Gorman
dc.authorsophosS., Hodgson
dc.authorsophosM.M.E., De Polanco
dc.authorsophosM., Sans
dc.authorsophosA., Carracedo
dc.authorsophosS., Castellvi-Bel
dc.authorsophosA., Rojas-Martinez
dc.authorsophosE., Santos
dc.authorsophosM.R., Teixeira
dc.authorsophosL., Carvajal-Carmona
dc.authorsophosX.-O., Shu
dc.authorsophosJ., Long
dc.authorsophosW., Zheng
dc.authorsophosY.-B., Xiang
dc.authorsophosG.W., Montgomery
dc.authorsophosP.M., Webb
dc.authorsophosR.J., Scott
dc.authorsophosM., McEvoy
dc.authorsophosJ., Attia
dc.authorsophosE., Holliday
dc.authorsophosN.G., Martin
dc.authorsophosD.R., Nyholt
dc.authorsophosA.K., Henders
dc.authorsophosP.A., Fasching
dc.authorsophosA., Hein
dc.authorsophosM.W., Beckmann
dc.authorsophosS.P., Renner
dc.authorsophosT., Dork
dc.authorsophosP., Hillemanns
dc.authorsophosM., Durst
dc.authorsophosI., Runnebaum
dc.authorsophosD., Lambrechts
dc.authorsophosL., Coenegrachts
dc.authorsophosS., Schrauwen
dc.authorsophosF., Amant
dc.authorsophosB., Winterhoff
dc.authorsophosS.C., Dowdy
dc.authorsophosE.L., Goode
dc.authorsophosA., Teoman
dc.authorsophosH.B., Salvesen
dc.authorsophosJ., Trovik
dc.authorsophosT.S., Njolstad
dc.authorsophosH.M.J., Werner
dc.authorsophosK., Ashton
dc.authorsophosT., Proietto
dc.authorsophosG., Otton
dc.authorsophosG., Tzortzatos
dc.authorsophosM., Mints
dc.authorsophosE., Tham
dc.authorsophosP., Hall
dc.authorsophosK., Czene
dc.authorsophosJ., Liu
dc.authorsophosJ., Li
dc.authorsophosJ.L., Hopper
dc.authorsophosM.C., Southey
dc.authorsophosA.B., Ekici
dc.authorsophosM., Ruebner
dc.authorsophosN., Johnson
dc.authorsophosJ., Peto
dc.authorsophosB., Burwinkel
dc.authorsophosF., Marme
dc.authorsophosH., Brenner
dc.authorsophosA.K., Dieffenbach
dc.authorsophosA., Meindl
dc.authorsophosH., Brauch
dc.authorsophosA., Lindblom
dc.authorsophosJ., Depreeuw
dc.authorsophosM., Moisse
dc.authorsophosJ., Chang-Claude
dc.authorsophosA., Rudolph
dc.authorsophosF.J., Couch
dc.authorsophosJ.E., Olson
dc.authorsophosG.G., Giles
dc.authorsophosF., Bruinsma
dc.authorsophosJ.M., Cunningham
dc.authorsophosB.L., Fridley
dc.authorsophosA.L., Borresen-Dale
dc.authorsophosV.N., Kristensen
dc.authorsophosA., Cox
dc.authorsophosA.J., Swerdlow
dc.authorsophosN., Orr
dc.authorsophosM.K., Bolla
dc.authorsophosQ., Wang
dc.authorsophosR.P., Weber
dc.authorsophosZ., Chen
dc.authorsophosM., Shah
dc.authorsophosJ.D., French
dc.authorsophosP.D.P., Pharoah
dc.authorsophosA.M., Dunning
dc.authorsophosI., Tomlinson
dc.authorsophosD.F., Easton
dc.authorsophosS.L., Edwards
dc.authorsophosD.J., Thompson
dc.authorsophosA.B., Spurdle
dc.identifier.doi10.1093/hmg/ddu552
dc.identifier.pmid25378557
dc.identifier.sophos19982
dc.issue.number5
dc.journal.titleHUMAN MOLECULAR GENETICS
dc.organizationConsellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.page.initial1478
dc.page.final1492
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number24


Ficheros en el ítem

FicherosTamañoFormatoVer

No hay ficheros asociados a este ítem.

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem