Search Results

There are 14832 results for: content related to: BRCA mutation-negative women from hereditary breast and ovarian cancer families: a qualitative study of the BRCA -negative experience

  1. You have free access to this content
    Significant proportion of breast and/or ovarian cancer families of French Canadian descent harbor 1 of 5 BRCA1 and BRCA2 mutations

    International Journal of Cancer

    Volume 112, Issue 3, 10 November 2004, Pages: 411–419, Kathleen K. Oros, Parviz Ghadirian, Celia M.T Greenwood, Chantal Perret, Zhen Shen, Yosabeth Paredes, Suzanna L. Arcand, Anne-Marie Mes-Masson, Steven A. Narod, William D. Foulkes, Diane Provencher and Patricia N. Tonin

    Article first published online : 23 JUN 2004, DOI: 10.1002/ijc.20406

  2. Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 3, March 2010, Pages: 674–686, Gabriel E. Zentner, Wanda S. Layman, Donna M. Martin and Peter C. Scacheri

    Article first published online : 22 FEB 2010, DOI: 10.1002/ajmg.a.33323

  3. Application of BRCA1 and BRCA2 mutation carrier prediction models in breast and/or ovarian cancer families of French Canadian descent

    Clinical Genetics

    Volume 70, Issue 4, October 2006, Pages: 320–329, KK Oros, P Ghadirian, CM Maugard, C Perret, Y Paredes, A-M Mes-Masson, WD Foulkes, D Provencher and PN Tonin

    Article first published online : 14 AUG 2006, DOI: 10.1111/j.1399-0004.2006.00673.x

  4. Genetic testing for hereditary colorectal cancer in children: Long-term psychological effects

    American Journal of Medical Genetics Part A

    Volume 116A, Issue 2, 15 January 2003, Pages: 117–128, Ann-Marie Codori, Kristin L. Zawacki, Gloria M. Petersen, Diana L. Miglioretti, Judith A. Bacon, Jill D. Trimbath, Susan V. Booker, Kimberly Picarello and Francis M. Giardiello

    Article first published online : 12 SEP 2002, DOI: 10.1002/ajmg.a.10926

  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

    Article first published online : 18 FEB 2013, DOI: 10.1111/cge.12091

  6. High prevalence of the G101W germline mutation in the CDKN2A (P16ink4a) gene in 62 Italian malignant melanoma families

    American Journal of Medical Genetics

    Volume 107, Issue 3, 22 January 2002, Pages: 214–221, Michela Mantelli, Monica Barile, Paola Ciotti, Paola Ghiorzo, Francesca Lantieri, Lorenza Pastorino, Caterina Catricalà, Gabriella Della Torre, Ugo Folco, Paola Grammatico, Laura Padovani, Barbara Pasini, Dario Rovini, Paola Queirolo, Maria Luisa Rainero, Pier Luigi Santi, Roberto M. Sertoli, Alisa M. Goldstein and Giovanna Bianchi-Scarrà

    Article first published online : 2 JAN 2002, DOI: 10.1002/ajmg.10137

  7. You have free access to this content
    Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer

    Cancer

    Volume 85, Issue 12, 15 June 1999, Pages: 2512–2518, Karl Heinimann, Rodney J. Scott, Jean-Marie Buerstedde, Walter Weber, Karl Siebold, Michèle Attenhofer, Hansjakob Müller and Zuzana Dobbie

    Article first published online : 19 NOV 2000, DOI: 10.1002/(SICI)1097-0142(19990615)85:12<2512::AID-CNCR4>3.0.CO;2-G

  8. BRAF mutation in follicular variant of papillary thyroid carcinoma is associated with unfavourable clinicopathological characteristics and malignant features on ultrasonography

    Clinical Endocrinology

    Volume 81, Issue 3, September 2014, Pages: 432–439, Young Jun Chai, Su-jin Kim, Soo Chin Kim, Do Hoon Koo, Hye Sook Min, Kyu Eun Lee, Ji-hoon Kim and Yeo-Kyu Youn

    Article first published online : 13 MAR 2014, DOI: 10.1111/cen.12433

  9. Exomic landscape of MED12 mutation-negative and -positive uterine leiomyomas

    International Journal of Cancer

    Volume 134, Issue 4, 15 February 2014, Pages: 1008–1012, Netta Mäkinen, Pia Vahteristo, Ralf Bützow, Jari Sjöberg and Lauri A. Aaltonen

    Article first published online : 29 AUG 2013, DOI: 10.1002/ijc.28410

  10. Evaluation of two different models to predict BRCA1 and BRCA2 mutations in a cohort of Danish hereditary breast and/or ovarian cancer families

    Clinical Genetics

    Volume 69, Issue 2, February 2006, Pages: 171–178, A-M Gerdes, DG Cruger, M Thomassen and TA Kruse

    Article first published online : 18 JAN 2006, DOI: 10.1111/j.1399-0004.2006.00568.x

  11. The identification of false positive responses to the pentagastrin stimulation test in RET mutation negative members of MEN 2A families

    Clinical Endocrinology

    Volume 44, Issue 2, February 1996, Pages: 213–220, Debbie J. Marsh, Deborah McDowall, Valentine J. Hyland, Scott D. Andrew, Margaret Schnitzler, Elizabeth L. Gaskin, David F. Nevell, Terrence Diamond, Leigh Delbridge, Phillip Clifton-Bligh and Bruce G. Robinson

    Article first published online : 29 OCT 2003, DOI: 10.1046/j.1365-2265.1996.505292.x

  12. You have free access to this content
    Psychological consequences of predictive genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): A prospective follow-up study

    International Journal of Cancer

    Volume 93, Issue 4, 15 August 2001, Pages: 608–611, Katja Aktan-Collan, Ari Haukkala, Jukka-Pekka Mecklin, Antti Uutela and Helena Kääriäinen

    Article first published online : 22 MAY 2001, DOI: 10.1002/ijc.1372

  13. Investigation of disease-associated factors in haemophilia A patients without detectable mutations

    Haemophilia

    Volume 18, Issue 3, May 2012, Pages: e132–e137, C. HALLDÉN, K. E. KNOBE, E. SJÖRIN, D. NILSSON and R. LJUNG

    Article first published online : 4 JAN 2012, DOI: 10.1111/j.1365-2516.2011.02737.x

  14. SPECT Study of the Nigrostriatal Dopaminergic System in Huntington's Disease

    Journal of Neuroimaging

    Volume 23, Issue 2, April 2013, Pages: 192–196, Wen-Juh Hwang and Wei-Jen Yao

    Article first published online : 30 DEC 2011, DOI: 10.1111/j.1552-6569.2011.00671.x

  15. You have full text access to this OnlineOpen article
    Driver mutations in TP53 are ubiquitous in high grade serous carcinoma of the ovary

    The Journal of Pathology

    Volume 221, Issue 1, May 2010, Pages: 49–56, Ahmed Ashour Ahmed, Dariush Etemadmoghadam, Jillian Temple, Andy G Lynch, Mohamed Riad, Raghwa Sharma, Colin Stewart, Sian Fereday, Carlos Caldas, Anna deFazio, David Bowtell and James D Brenton

    Article first published online : 3 FEB 2010, DOI: 10.1002/path.2696

  16. Papillary thyroid carcinomas with and without BRAF  V600E mutations are morphologically distinct

    Histopathology

    Volume 60, Issue 7, June 2012, Pages: 1052–1059, Alexander Finkelstein, Gillian H Levy, Pei Hui, Avinash Prasad, Renu Virk, David C Chhieng, Tobias Carling, Sanziana A Roman, Julie A Sosa, Robert Udelsman, Constantine G Theoharis and Manju L Prasad

    Article first published online : 15 FEB 2012, DOI: 10.1111/j.1365-2559.2011.04149.x

  17. You have free access to this content
    Changes in serum cartilage marker levels indicate altered cartilage metabolism in families with the osteoarthritis-related type II collagen gene COL2A1 mutation

    Arthritis & Rheumatism

    Volume 42, Issue 1, January 1999, Pages: 39–45, Jane F. Bleasel, A. Robin Poole, Dick Heinegård, Tore Saxne, Daniel Holderbaum, Mirella Ionescu, Paul Jones and Roland W. Moskowitz

    Article first published online : 22 MAY 2001, DOI: 10.1002/1529-0131(199901)42:1<39::AID-ANR5>3.0.CO;2-Y

  18. Mutational and genotype–phenotype correlation analyses in 28 Polish patients with Cornelia de Lange syndrome

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 14, 15 July 2006, Pages: 1531–1541, Jiong Yan, Gulam Mustafa Saifi, Tomasz H. Wierzba, Marjorie Withers, Gabriel A. Bien-Willner, Janusz Limon, Paweł Stankiewicz, James R. Lupski and Jolanta Wierzba

    Article first published online : 12 JUN 2006, DOI: 10.1002/ajmg.a.31305

  19. Sensitive KIT D816V mutation analysis of blood as a diagnostic test in mastocytosis

    American Journal of Hematology

    Volume 89, Issue 5, May 2014, Pages: 493–498, Thomas Kristensen, Hanne Vestergaard, Carsten Bindslev-Jensen, Michael Boe Møller, Sigurd Broesby-Olsen and on Behalf of the Mastocytosis Centre Odense University Hospital (MastOUH)

    Article first published online : 21 FEB 2014, DOI: 10.1002/ajh.23672

  20. Competing Risks Analysis of Correlated Failure Time Data

    Biometrics

    Volume 64, Issue 1, March 2008, Pages: 172–179, Bingshu E. Chen, Joan L. Kramer, Mark H. Greene and Philip S. Rosenberg

    Article first published online : 3 AUG 2007, DOI: 10.1111/j.1541-0420.2007.00868.x