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Refinado por: assunto: Breast Neoplasms - Genetics remover
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BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk
BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk
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BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk

Spurdle, Amanda B ; Whiley, Phillip J ; Thompson, Bryony ; Feng, Bingjian ; Healey, Sue ; Brown, Melissa A ; Pettigrew, Christopher ; Van Asperen, Christi J ; Ausems, Margreet G E M ; Kattentidt-Mouravieva, Anna A ; van den Ouweland, Ans M W ; Belgium UV Consortium, Dutch ; Lindblom, Annika ; Pigg, Maritta H ; Schmutzler, Rita K ; Engel, Christoph ; Meindl, Alfons ; Caputo, Sandrine ; Sinilnikova, Olga M ; Lidereau, Rosette ; Couch, Fergus J ; Guidugli, Lucia ; Hansen, Thomas van Overeem ; Thomassen, Mads ; Eccles, Diana M ; Tucker, Kathy ; Benitez, Javier ; Domchek, Susan M ; Toland, Amanda E ; Van Rensburg, Elizabeth J ; Wappenschmidt, Barbara ; Borg, Åke ; Vreeswijk, Maaike P G ; Goldgar, David E

Journal of medical genetics, 2012-08, Vol.49 (8), p.525-532 [Periódico revisado por pares]

England: BMJ Publishing Group Ltd

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2
The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers
The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers
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The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

Garcia, Amandine I. ; Cox, David G. ; Barjhoux, Laure ; Verny-Pierre, Carole ; Barnes, Daniel ; Antoniou, Antonis C. ; Stoppa-Lyonnet, Dominique ; Sinilnikova, Olga M. ; Mazoyer, Sylvie

Human mutation, 2011-09, Vol.32 (9), p.1004-1007 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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3
Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers
Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers
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Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers

SPURDLE, Amanda B ; MARQUART, Louise ; GSCHWANTLER-KAULICH, Daphne ; BLUM, Joanne L ; TUNG, Nadine ; WEITZEL, Jeff ; LYNCH, Henry ; GARBER, Judy ; EASTON, Douglas F ; PEOCK, Susan ; COOK, Margaret ; OLIVER, Clare T ; MCGUFFOG, Lesley ; FROST, Debra ; CONROY, Don ; GARETH EVANS, D ; LALLOO, Fiona ; EELES, Ros ; IZATT, Louise ; DAVIDSON, Rosemarie ; CHU, Carol ; ECCLES, Diana ; SELKIRK, Christina G ; HEALEY, Sue ; DALY, Mary ; ISAACS, Claudine ; STOPPA-LYONNET, Dominique ; SINILNIKOVA, Olga M ; BUECHER, Bruno ; BELOTTI, Muriel ; MAZOYER, Sylvie ; BARJHOUX, Laure ; VERNY-PIERRE, Carole ; LASSET, Christine ; SINILNIKOVA, Olga ; DREYFUS, Hélène ; PUJOL, Pascal ; COLLONGE-RAME, Marie-Agnès ; ROOKUS, Matti A ; VERHOEF, Senno ; KRIEGE, Mieke ; HOOGERBRUGGE, Nicoline ; AUSEMS, Margreet G. E. M ; VAN OS, Theo A ; WIJNEN, Juul ; FEI WAN ; DEVILEE, Peter ; MEIJERS-HEIJBOER, Hanne E. J ; BLOK, Marinus J ; HEIKKINEN, Tuomas ; NEVANLINNA, Heli ; JAKUBOWSKA, Anna ; LUBINSKI, Jan ; HUZARSKI, Tomasz ; BYRSKI, Tomasz ; DUROCHER, Francine ; XIAOQING CHEN ; BEESLEY, Jonathan ; SINGER, Christian F ; DRESSLER, Anne-Catharine

Cancer epidemiology, biomarkers & prevention, 2011, Vol.20 (5), p.1032-1038 [Periódico revisado por pares]

Philadelphia, PA: American Association for Cancer Research

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  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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