Search Results

There are 34929 results for: content related to: Impact of gynecological screening in Lynch syndrome carriers with an MSH2 mutation

  1. Epigenetic mechanisms in the pathogenesis of Lynch syndrome

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 403–412, P. Peltomäki

    Version of Record online : 17 FEB 2014, DOI: 10.1111/cge.12349

  2. Impact of colonoscopic screening in male and female Lynch syndrome carriers with an MSH2 mutation

    Clinical Genetics

    Volume 82, Issue 5, November 2012, Pages: 439–445, S Stuckless, JS Green, M Morgenstern, C Kennedy, RC Green, MO Woods, W Fitzgerald, J Cox and PS Parfrey

    Version of Record online : 15 NOV 2011, DOI: 10.1111/j.1399-0004.2011.01802.x

  3. Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome

    Clinical Genetics

    Volume 87, Issue 6, June 2015, Pages: 507–516, G. Ponti, E. Castellsagué, C. Ruini, A. Percesepe and A. Tomasi

    Version of Record online : 9 DEC 2014, DOI: 10.1111/cge.12529

  4. Gynecologic cancer screening and communication with health care providers in women with Lynch syndrome

    Clinical Genetics

    Volume 86, Issue 2, August 2014, Pages: 185–189, A.M. Burton-Chase, S.R. Hovick, C.C. Sun, S. Boyd-Rogers, P.M. Lynch, K.H. Lu and S.K. Peterson

    Version of Record online : 27 AUG 2013, DOI: 10.1111/cge.12246

  5. Changes in screening behaviors and attitudes toward screening from pre-test genetic counseling to post-disclosure in Lynch syndrome families

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 215–220, AM Burton-Chase, SR Hovick, SK Peterson, SK Marani, SW Vernon, CI Amos, ML Frazier, PM Lynch and ER Gritz

    Version of Record online : 18 FEB 2013, DOI: 10.1111/cge.12091

  6. Improving the uptake of predictive testing and colorectal screening in Lynch syndrome: a regional primary care survey

    Clinical Genetics

    Volume 87, Issue 6, June 2015, Pages: 517–524, P. Barrow, K. Green, T. Clancy, F. Lalloo, J. Hill and D.G. Evans

    Version of Record online : 4 FEB 2015, DOI: 10.1111/cge.12559

  7. Colonoscopy screening compliance and outcomes in patients with Lynch syndrome

    Colorectal Disease

    Volume 17, Issue 1, January 2015, Pages: 38–46, K. Newton, K. Green, F. Lalloo, D. G. Evans and J. Hill

    Version of Record online : 23 DEC 2014, DOI: 10.1111/codi.12778

  8. The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families

    Clinical Genetics

    Volume 84, Issue 3, September 2013, Pages: 244–250, M Pinheiro, C Pinto, A Peixoto, I Veiga, B Mesquita, R Henrique, P Lopes, O Sousa, M Fragoso, LM Dias, M Baptista, C Marinho, E Mangold, C Vaccaro, DG Evans, S Farrington, MG Dunlop and MR MR Teixeira

    Version of Record online : 27 DEC 2012, DOI: 10.1111/cge.12062

  9. A review of mismatch repair gene transcripts: issues for interpretation of mRNA splicing assays

    Clinical Genetics

    Volume 87, Issue 2, February 2015, Pages: 100–108, B.A. Thompson, A. Martins and A.B. Spurdle

    Version of Record online : 26 JUL 2014, DOI: 10.1111/cge.12450

  10. You have full text access to this OnlineOpen article
    Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory

    Clinical Genetics

    Volume 86, Issue 6, December 2014, Pages: 510–520, D. Cragun, C. Radford, J.S. Dolinsky, M. Caldwell, E. Chao and T. Pal

    Version of Record online : 20 MAR 2014, DOI: 10.1111/cge.12359

  11. Recurrent and founder mutations in the PMS2 gene

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 238–243, J Tomsic, L Senter, S Liyanarachchi, M Clendenning, C P Vaughn, M A Jenkins, J L Hopper, J Young, W Samowitz and A de la Chapelle

    Version of Record online : 4 JUN 2012, DOI: 10.1111/j.1399-0004.2012.01898.x

  12. Long-term psychosocial and behavioral adjustment in individuals receiving genetic test results in Lynch syndrome

    Clinical Genetics

    Volume 87, Issue 6, June 2015, Pages: 525–532, M.J. Esplen, J. Wong, M. Aronson, K. Butler, H. Rothenmund, K. Semotiuk, L. Madlensky, C. Way, E. Dicks, J. Green and S. Gallinger

    Version of Record online : 28 OCT 2014, DOI: 10.1111/cge.12509

  13. BRCA1 and BRCA2 mutations and the risk for colorectal cancer

    Clinical Genetics

    Volume 87, Issue 5, May 2015, Pages: 411–418, V. Sopik, C. Phelan, C. Cybulski and S.A. Narod

    Version of Record online : 21 OCT 2014, DOI: 10.1111/cge.12497

  14. Dawning of the epigenetic era in hereditary cancer

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 413–416, M.P. Hitchins and H.T. Lynch

    Version of Record online : 1 APR 2014, DOI: 10.1111/cge.12369

  15. Identification of a founder EPCAM deletion in Spanish Lynch syndrome families

    Clinical Genetics

    Volume 85, Issue 3, March 2014, Pages: 260–266, P. Mur, M. Pineda, A. Romero, J. del Valle, E. Borràs, A. Canal, M. Navarro, J. Brunet, D. Rueda, T. Ramón y Cajal, C. Lázaro, T. Caldés, I. Blanco, J.L. Soto and G. Capellá

    Version of Record online : 26 APR 2013, DOI: 10.1111/cge.12152

  16. You have free access to this content
    Lynch syndrome: five unanswered questions

    Clinical Genetics

    Volume 87, Issue 6, June 2015, Pages: 503–506, E. Castellsagué and W.D. Foulkes

    Version of Record online : 5 MAY 2015, DOI: 10.1111/cge.12580

  17. Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population

    Clinical Genetics

    Volume 87, Issue 6, June 2015, Pages: 536–542, E. Castellsagué, J. Liu, A. Volenik, S. Giroux, R. Gagné, B. Maranda, A. Roussel-Jobin, J. Latreille, R. Laframboise, L. Palma, L. Kasprzak, V.A. Marcus, M. Breguet, S. Nolet, Z. El-Haffaf, K. Australie, A. Gologan, O. Aleynikova, K. Oros-Klein, C. Greenwood, A.M. Mes-Masson, D. Provencher, M. Tischkowitz, G. Chong, F. Rousseau and W.D. Foulkes

    Version of Record online : 22 NOV 2014, DOI: 10.1111/cge.12526

  18. Genetic testing for RAD51C mutations: in the clinic and community

    Clinical Genetics

    Volume 88, Issue 4, October 2015, Pages: 303–312, V. Sopik, M.R. Akbari and S.A. Narod

    Version of Record online : 7 JAN 2015, DOI: 10.1111/cge.12548

  19. High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families

    Clinical Genetics

    Volume 85, Issue 6, June 2014, Pages: 583–588, A.J. Brea-Fernández, J.M. Cameselle-Teijeiro, C. Alenda, C. Fernández-Rozadilla, J. Cubiella, J. Clofent, J.M. Reñé, U. Anido, M. Milá, F. Balaguer, A. Castells, S. Castellvi-Bel, R. Jover, A. Carracedo and C. Ruiz-Ponte

    Version of Record online : 28 JUL 2013, DOI: 10.1111/cge.12232

  20. Communication and technology in genetic counseling for familial cancer

    Clinical Genetics

    Volume 85, Issue 3, March 2014, Pages: 213–222, H.T. Lynch, C. Snyder, M. Stacey, B. Olson, S.K. Peterson, S. Buxbaum, T. Shaw and P.M. Lynch

    Version of Record online : 20 DEC 2013, DOI: 10.1111/cge.12317