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
  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. 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

      Version of Record 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
  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. 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

      Version of Record 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. 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

      Version of Record online: 20 OCT 2013 | DOI: 10.1111/cge.12274

    2. 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

      Version of Record online: 21 MAR 2013 | DOI: 10.1111/cge.12130

    3. Linking distant relatives with BRCA gene mutations: potential for cost savings (pages 54–58)

      L Senter, M O'Connor, F Oriyo, K Sweet and AE Toland

      Version of Record online: 24 JUN 2013 | DOI: 10.1111/cge.12211

    4. 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

      Version of Record online: 11 MAR 2013 | DOI: 10.1111/cge.12119

    5. 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

      Version of Record online: 5 APR 2013 | DOI: 10.1111/cge.12132

    6. 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

      Version of Record online: 9 APR 2013 | DOI: 10.1111/cge.12149

    7. 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

      Version of Record 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
  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. 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

      Version of Record online: 27 MAR 2013 | DOI: 10.1111/cge.12090

    2. 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

      Version of Record 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. 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

      Version of Record online: 17 MAR 2013 | DOI: 10.1111/cge.12122

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