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Clinical Genetics

Cover image for Vol. 85 Issue 1

Special Issue: BRCA1 and BRCA2

January 2014

Volume 85, Issue 1

Pages 1–99

  1. COMMENTARIES

    1. Top of page
    2. COMMENTARIES
    3. SOCIAL AND BEHAVIOURAL RESEARCH IN CLINICAL GENETICS
    4. HOTSPOTS
    5. ORIGINAL ARTICLES
    6. SHORT REPORTS
    7. COMMENTARY
    8. ORIGINAL ARTICLES
    9. LETTER TO THE EDITOR
    1. You have free access to this content
    2. You have free access to this content
  2. SOCIAL AND BEHAVIOURAL RESEARCH IN CLINICAL GENETICS

    1. Top of page
    2. COMMENTARIES
    3. SOCIAL AND BEHAVIOURAL RESEARCH IN CLINICAL GENETICS
    4. HOTSPOTS
    5. ORIGINAL ARTICLES
    6. SHORT REPORTS
    7. COMMENTARY
    8. ORIGINAL ARTICLES
    9. LETTER TO THE EDITOR
    1. You have free access to this content
      The psychological impact of breast and ovarian cancer preventive options in BRCA1 and BRCA2 mutation carriers (pages 7–15)

      C Borreani, S Manoukian, E Bianchi, C Brunelli, B Peissel, A Caruso, G Morasso and MA Pierotti

      Article first published online: 5 NOV 2013 | DOI: 10.1111/cge.12298

      Section Editor:

      Aad Tibben, email: a.tibben@lumc.nl

  3. HOTSPOTS

    1. Top of page
    2. COMMENTARIES
    3. SOCIAL AND BEHAVIOURAL RESEARCH IN CLINICAL GENETICS
    4. HOTSPOTS
    5. ORIGINAL ARTICLES
    6. SHORT REPORTS
    7. COMMENTARY
    8. ORIGINAL ARTICLES
    9. LETTER TO THE EDITOR
    1. You have free access to this content
    2. You have free access to this content
    3. You have free access to this content
  4. ORIGINAL ARTICLES

    1. Top of page
    2. COMMENTARIES
    3. SOCIAL AND BEHAVIOURAL RESEARCH IN CLINICAL GENETICS
    4. HOTSPOTS
    5. ORIGINAL ARTICLES
    6. SHORT REPORTS
    7. COMMENTARY
    8. ORIGINAL ARTICLES
    9. LETTER TO THE EDITOR
    1. You have free access to this content
    2. You have free access to this content
      Screening for BRCA1 and BRCA2 mutations among French-Canadian breast cancer cases attending an outpatient clinic in Montreal (pages 31–35)

      P Ghadirian, A Robidoux, E Nassif, G Martin, C Potvin, E Patocskai, R Younan, N Larouche, A Venne, S Zhang, R Royer and SA Narod

      Article first published online: 5 JUN 2013 | DOI: 10.1111/cge.12174

  5. SHORT REPORTS

    1. Top of page
    2. COMMENTARIES
    3. SOCIAL AND BEHAVIOURAL RESEARCH IN CLINICAL GENETICS
    4. HOTSPOTS
    5. ORIGINAL ARTICLES
    6. SHORT REPORTS
    7. COMMENTARY
    8. ORIGINAL ARTICLES
    9. LETTER TO THE EDITOR
    1. You have free access to this content
      High prevalence of BRCA1 founder mutations in Greek breast/ovarian families (pages 36–42)

      I Konstantopoulou, M Tsitlaidou, F Fostira, M Pertesi, A-V Stavropoulou, O Triantafyllidou, E Tsotra, AP Tsiftsoglou, C Tsionou, S Droufakou, C Dimitrakakis, G Fountzilas and D Yannoukakos

      Article first published online: 20 OCT 2013 | DOI: 10.1111/cge.12274

    2. You have free access to this content
    3. You have free access to this content
      Modes of delivery of genetic testing services and the uptake of cancer risk management strategies in BRCA1 and BRCA2 carriers (pages 49–53)

      T Pal, J-H Lee, A Besharat, Z Thompson, ANA Monteiro, C Phelan, JM Lancaster, K Metcalfe, TA Sellers, S Vadaparampil and SA Narod

      Article first published online: 21 MAR 2013 | DOI: 10.1111/cge.12130

    4. You have free access to this content
    5. You have free access to this content
      Geographical distribution of Slovenian BRCA1/2 families according to family origin: implications for genetic screening (pages 59–63)

      M Krajc, V Zadnik, S Novaković, V Stegel, E Teugels, N Bešič, M Hočevar, A Vakselj, J De Grève and J Žgajnar

      Article first published online: 11 MAR 2013 | DOI: 10.1111/cge.12119

    6. You have free access to this content
      The spectrum of BRCA1 and BRCA2 mutations in breast cancer patients in the Bahamas (pages 64–67)

      MR Akbari, T Donenberg, J Lunn, D Curling, T Turnquest, E Krill-Jackson, S Zhang, SA Narod and J Hurley

      Article first published online: 5 APR 2013 | DOI: 10.1111/cge.12132

    7. You have free access to this content
      Rates of risk-reducing surgery in Israeli BRCA1 and BRCA2 mutation carriers (pages 68–71)

      Y Laitman, Y Vaisman, D Feldman, L Helpman, M Gitly, S Paluch Shimon, R Berger, L Cohen, SA Narod and E Friedman

      Article first published online: 9 APR 2013 | DOI: 10.1111/cge.12149

    8. You have free access to this content
      Clinical implications of genetic testing for BRCA1 and BRCA2 mutations in Austria (pages 72–75)

      CF Singer, D Muhr, C Rappaport, M-K Tea, D Gschwantler-Kaulich, A Fink-Retter, G Pfeiler, A Berger, P Sun and SA Narod

      Article first published online: 16 JUL 2013 | DOI: 10.1111/cge.12216

  6. COMMENTARY

    1. Top of page
    2. COMMENTARIES
    3. SOCIAL AND BEHAVIOURAL RESEARCH IN CLINICAL GENETICS
    4. HOTSPOTS
    5. ORIGINAL ARTICLES
    6. SHORT REPORTS
    7. COMMENTARY
    8. ORIGINAL ARTICLES
    9. LETTER TO THE EDITOR
    1. You have free access to this content
  7. ORIGINAL ARTICLES

    1. Top of page
    2. COMMENTARIES
    3. SOCIAL AND BEHAVIOURAL RESEARCH IN CLINICAL GENETICS
    4. HOTSPOTS
    5. ORIGINAL ARTICLES
    6. SHORT REPORTS
    7. COMMENTARY
    8. ORIGINAL ARTICLES
    9. LETTER TO THE EDITOR
    1. You have free access to this content
      Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008 (pages 78–86)

      MC van Rij, PAM de Koning Gans, CM Aalfs, M Elting, PF Ippel, JA Maat-Kievit, S Vermeer, CC Verschuuren-Bemelmans, MJ van Belzen, RDM Belfroid, M Losekoot, JPM Geraedts, RAC Roos, A Tibben, CEM de Die-Smulders and EK Bijlsma

      Article first published online: 27 MAR 2013 | DOI: 10.1111/cge.12090

    2. You have free access to this content
      The uptake and outcome of prenatal and pre-implantation genetic diagnosis for Huntington's disease in the Netherlands (1998–2008) (pages 87–95)

      MC van Rij, PAM de Koning Gans, MJ van Belzen, RAC Roos, JPM Geraedts, M De Rademaeker, EK Bijlsma and CEM de Die-Smulders

      Article first published online: 21 MAR 2013 | DOI: 10.1111/cge.12089

  8. LETTER TO THE EDITOR

    1. Top of page
    2. COMMENTARIES
    3. SOCIAL AND BEHAVIOURAL RESEARCH IN CLINICAL GENETICS
    4. HOTSPOTS
    5. ORIGINAL ARTICLES
    6. SHORT REPORTS
    7. COMMENTARY
    8. ORIGINAL ARTICLES
    9. LETTER TO THE EDITOR
    1. You have free access to this content
      RSK2 mutation co-segregates with X-linked intellectual disability and attenuated Coffin–Lowry phenotype in a three-generation family (pages 96–99)

      I Maystadt, A Destree, V Benoit, A Aeby, D Lederer, S Moortgat, D Jurkiewicz, M Krajewska-Walasek, A Hanauer and GM Thomas

      Article first published online: 17 MAR 2013 | DOI: 10.1111/cge.12122

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