Clinical Genetics

Cover image for Vol. 86 Issue 1

Special Issue: Personalized Medicine and Clinical Genetics

July 2014

Volume 86, Issue 1

Pages 1–101

  1. Announcement

    1. Top of page
    2. Announcement
    3. REVIEWS
    4. ORIGINAL ARTICLES
    5. SHORT REPORT
    6. LETTERS TO THE EDITOR
    1. Developmental Biology: Frontiers for Clinical Genetics

      Michael R. Hayden

      Version of Record online: 3 JUN 2014 | DOI: 10.1111/cge.12429

  2. REVIEWS

    1. Top of page
    2. Announcement
    3. REVIEWS
    4. ORIGINAL ARTICLES
    5. SHORT REPORT
    6. LETTERS TO THE EDITOR
    1. You have full text access to this OnlineOpen article
      Personalized ophthalmology (pages 1–11)

      L.F. Porter and G.C.M. Black

      Version of Record online: 3 JUN 2014 | DOI: 10.1111/cge.12389

    2. You have full text access to this OnlineOpen article
      The emerging era of pharmacogenomics: current successes, future potential, and challenges (pages 21–28)

      J.W. Lee, F. Aminkeng, A.P. Bhavsar, K. Shaw, B.C. Carleton, M.R. Hayden and C.J.D. Ross

      Version of Record online: 9 MAY 2014 | DOI: 10.1111/cge.12392

    3. You have free access to this content
      Personalized gene silencing therapeutics for Huntington disease (pages 29–36)

      C. Kay, N.H. Skotte, A.L. Southwell and M.R. Hayden

      Version of Record online: 11 APR 2014 | DOI: 10.1111/cge.12385

    4. Innovative personalized medicine in gastric cancer: time to move forward (pages 37–43)

      J. Lee, K.-M. Kim, W.K. Kang and S.-H.I. Ou

      Version of Record online: 10 MAY 2014 | DOI: 10.1111/cge.12408

    5. You have full text access to this OnlineOpen article
    6. You have free access to this content
      Biobanks and personalized medicine (pages 50–55)

      J.E. Olson, S.J. Bielinski, E. Ryu, E.M. Winkler, P.Y. Takahashi, J. Pathak and J.R. Cerhan

      Version of Record online: 27 MAR 2014 | DOI: 10.1111/cge.12370

    7. You have free access to this content
      The beginning of personalized medicine in sepsis: small steps to a bright future (pages 56–61)

      E. Christaki and E.J. Giamarellos-Bourboulis

      Version of Record online: 27 MAR 2014 | DOI: 10.1111/cge.12368

    8. You have free access to this content
      Personalized therapy for breast cancer (pages 62–67)

      F.B. De Abreu, G.N. Schwartz, W.A. Wells and G.J. Tsongalis

      Version of Record online: 9 APR 2014 | DOI: 10.1111/cge.12381

    9. You have free access to this content
      MicroRNAs in personalized cancer therapy (pages 68–73)

      S. Sethi, S. Ali, S. Sethi and F.H. Sarkar

      Version of Record online: 20 MAR 2014 | DOI: 10.1111/cge.12362

  3. ORIGINAL ARTICLES

    1. Top of page
    2. Announcement
    3. REVIEWS
    4. ORIGINAL ARTICLES
    5. SHORT REPORT
    6. LETTERS TO THE EDITOR
    1. Phenotype–genotype correlations in patients with Marinesco–Sjögren syndrome (pages 74–84)

      F. Ezgu, P. Krejci, S. Li, C. de Sousa, J.M. Graham Jr, I. Hansmann, W. He, K. Porpora, D. Wand, W. Wertelecki, A. Schneider and W.R. Wilcox

      Version of Record online: 30 JUL 2013 | DOI: 10.1111/cge.12230

    2. LQTS in Northern BC: homozygosity for KCNQ1 V205M presents with a more severe cardiac phenotype but with minimal impact on auditory function (pages 85–90)

      H.A. Jackson, S. McIntosh, B. Whittome, S. Asuri, B. Casey, C. Kerr, A. Tang and L.T. Arbour

      Version of Record online: 30 JUL 2013 | DOI: 10.1111/cge.12235

  4. SHORT REPORT

    1. Top of page
    2. Announcement
    3. REVIEWS
    4. ORIGINAL ARTICLES
    5. SHORT REPORT
    6. LETTERS TO THE EDITOR
    1. Extensive sequence analysis of CFTR, SCNN1A, SCNN1B, SCNN1G and SERPINA1 suggests an oligogenic basis for cystic fibrosis-like phenotypes (pages 91–95)

      M.D. Ramos, D. Trujillano, R. Olivar, F. Sotillo, S. Ossowski, J. Manzanares, J. Costa, S. Gartner, C. Oliva, E. Quintana, M.I. Gonzalez, C. Vazquez, X. Estivill and T. Casals

      Version of Record online: 28 JUL 2013 | DOI: 10.1111/cge.12234

  5. LETTERS TO THE EDITOR

    1. Top of page
    2. Announcement
    3. REVIEWS
    4. ORIGINAL ARTICLES
    5. SHORT REPORT
    6. LETTERS TO THE EDITOR
    1. Large normal alleles and SCA2 prevalence: lessons from a nationwide study and analysis of the literature (pages 96–98)

      J.M. Laffita-Mesa, L.E. Almaguer-Mederos, V. Kourí, P.O. Bauer, Y. Vázquez-Mojena, T. Cruz Mariño and L. Velázquez-Pérez

      Version of Record online: 18 JUL 2013 | DOI: 10.1111/cge.12221

    2. Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I (pages 99–101)

      S. Assereto, A. Robbiano, M. Di Rocco, A. Rossi, D. Cassandrini, C. Panicucci, G. Brigati, R. Biancheri, C. Bruno, C. Minetti, H. Trucks, T. Sander, F. Zara and E. Gazzerro

      Version of Record online: 11 SEP 2013 | DOI: 10.1111/cge.12248

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