Clinical Genetics

Cover image for Clinical Genetics

October 2003

Volume 64, Issue 4

Pages 269–375

  1. Mini Review

    1. Top of page
    2. Mini Review
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Hotspots
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Errata
    1. Niemann–Pick disease type C (pages 269–281)

      MT Vanier and G Millat

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.00147.x

  2. Developmental Biology: Frontiers for Clinical Genetics

    1. Top of page
    2. Mini Review
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Hotspots
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Errata
  3. Hotspots

    1. Top of page
    2. Mini Review
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Hotspots
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Errata
    1. A new locus for inheritance of malignant melanoma (pages 293–296)

      SE Andrew

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.01563.x

    2. Redefining xeroderma pigmentosum complementation group E (pages 293–296)

      SE Andrew

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.01562.x

  4. Images in Genetics

    1. Top of page
    2. Mini Review
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Hotspots
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Errata
  5. Original Articles

    1. Top of page
    2. Mini Review
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Hotspots
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Errata
    1. Psychological consequences and predictors of adverse events in the first 5 years after predictive testing for Huntington's disease (pages 300–309)

      EW Almqvist, RR Brinkman, S Wiggins, MR Hayden and The Canadian Collaborative Study of Predictive Testing

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.00157.x

    2. Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality (pages 310–316)

      HA Heilstedt, BC Ballif, LA Howard, CD Kashork and LG Shaffer

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.00126.x

    3. To tell or not to tell: barriers and facilitators in family communication about genetic risk (pages 317–326)

      K Forrest, SA Simpson, BJ Wilson, ER Van Teijlingen, L McKee, N Haites and E Matthews

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.00142.x

    4. Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy (pages 339–349)

      J Erdmann, S Daehmlow, S Wischke, M Senyuva, U Werner, J Raible, N Tanis, S Dyachenko, M Hummel, R Hetzer and V Regitz-Zagrosek

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.00151.x

  6. Short Reports

    1. Top of page
    2. Mini Review
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Hotspots
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Errata
    1. Split hand foot malformation is associated with a reduced level of Dactylin gene expression (pages 350–354)

      D Basel, A DePaepe, MW Kilpatrick and P Tsipouras

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.00153.x

    2. Use of cancer susceptibility testing among primary care physicians (pages 355–360)

      R Sifri, R Myers, T Hyslop, B Turner, J Cocroft, T Rothermel, J Grana and N Schlackman

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.00131.x

    3. Ring chromosome 17: phenotype variation by deletion size (pages 361–365)

      V Shashi, JR White, MJ Pettenati, SK Root and WL Bell

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.00146.x

    4. The effects of the Pro12Ala polymorphism of the PPARγ-2 gene on lipid metabolism interact with body size at birth (pages 366–370)

      J Eriksson, V Lindi, M Uusitupa, T Forsén, M Laakso, C Osmond and D Barker

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.00150.x

  7. Letter to the Editor

    1. Top of page
    2. Mini Review
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Hotspots
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Errata
  8. Errata

    1. Top of page
    2. Mini Review
    3. Developmental Biology: Frontiers for Clinical Genetics
    4. Hotspots
    5. Images in Genetics
    6. Original Articles
    7. Short Reports
    8. Letter to the Editor
    9. Errata
    1. You have free access to this content
      Errata (page 375)

      Version of Record online: 15 SEP 2003 | DOI: 10.1034/j.1399-0004.2003.00170.x

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