Clinical Genetics

Cover image for Clinical Genetics

August 2002

Volume 62, Issue 2

Pages 97–191

  1. Mini Review

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcement
    1. Epigenetic contributors to the discordance of monozygotic twins (pages 97–103)

      SM Singh, B Murphy and R O'Reilly

      Version of Record online: 6 SEP 2002 | DOI: 10.1034/j.1399-0004.2002.620201.x

  2. Hotspots

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcement
    1. HotSpots (pages 104–109)

      ME Suzanne Lewis

      Version of Record online: 6 SEP 2002 | DOI: 10.1034/j.1399-0004.2002.620202.x

  3. Original Article

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcement
    1. Living with Marfan syndrome III. Quality of life and reproductive planning (pages 110–120)

      KF Peters, F Kong, M Hanslo and BB Biesecker

      Version of Record online: 6 SEP 2002 | DOI: 10.1034/j.1399-0004.2002.620203.x

    2. Family issues in a psychoeducation group for women with a BRCA mutation (pages 121–127)

      J Speice, SH McDaniel, PT Rowley and S Loader

      Version of Record online: 6 SEP 2002 | DOI: 10.1034/j.1399-0004.2002.620204.x

  4. Short Report

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcement
    1. Anticipation in hereditary breast cancer (pages 147–150)

      E Dagan and R Gershoni-Baruch

      Version of Record online: 6 SEP 2002 | DOI: 10.1034/j.1399-0004.2002.620207.x

    2. Haplotype analysis of a BRCA1: 185delAG mutation in a Chilean family supports its Ashkenazi origins (pages 151–156)

      N Ah Mew, N Hamel, M Galvez, M Al-Saffar and WD Foulkes

      Version of Record online: 6 SEP 2002 | DOI: 10.1034/j.1399-0004.2002.620208.x

    3. Craniofacial features in Cohen syndrome: an anthropometric and cephalometric analysis of 14 patients (pages 157–164)

      K Hurmerinta, S Pirinen, O Kovero and S Kivitie-Kallio

      Version of Record online: 6 SEP 2002 | DOI: 10.1034/j.1399-0004.2002.620209.x

    4. Spinal muscular atrophy in black South Africans: concordance with the universal SMN1 genotype (pages 165–168)

      J M Wilmshurst, L Reynolds, R Van Toorn, F Leisegang and H E Henderson

      Version of Record online: 6 SEP 2002 | DOI: 10.1034/j.1399-0004.2002.620210.x

    5. Three novel mutations of the PKD1 gene in Korean patients with autosomal dominant polycystic kidney disease (pages 169–174)

      H-S Eo, JG Lee, C Ahn, JT Cho, DY Hwang, YH Hwang, EJ Lee, YS Kim, JS Han, S Kim, JS Lee, DI Jeoung, SE Lee and UK Kim

      Version of Record online: 6 SEP 2002 | DOI: 10.1034/j.1399-0004.2002.620211.x

  5. Letter to the Editor

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcement
    1. How many phenotypes in the DTDST family chondrodysplasias? (pages 189–190)

      A Mégarbané, I Farkh and S Haddad-Zebouni

      Version of Record online: 6 SEP 2002 | DOI: 10.1034/j.1399-0004.2002.620214.x

  6. Announcement

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Original Article
    5. Short Report
    6. Letter to the Editor
    7. Announcement
    1. CALL FOR ABSTRACTS (page 191)

      Version of Record online: 6 SEP 2002 | DOI: 10.1034/j.1399-0004.2002.620215.x

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