Clinical Genetics

Cover image for Clinical Genetics

March 2003

Volume 63, Issue 3

Pages 169–240

  1. Mini Review

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. Genetic counseling for prostate cancer risk (pages 169–176)

      AM Nieder, SS Taneja, MPA Zeegers and H Ostrer

      Version of Record online: 12 APR 2003 | DOI: 10.1034/j.1399-0004.2003.00038.x

  2. Hotspots

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
  3. Original Articles

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. The allelic loss of chromosome 3p25 with c-myc gain is related to the development of clear-cell renal cell carcinoma (pages 184–191)

      S Yamaguchi, S Yoshihiro, H Matsuyama, K Nagao, K Fukunaga, H Matsumoto, K Matsuda, K Oba and K Naito

      Version of Record online: 12 APR 2003 | DOI: 10.1034/j.1399-0004.2003.00035.x

    2. The natural history of sclerosteosis (pages 192–197)

      H Hamersma, J Gardner and P Beighton

      Version of Record online: 12 APR 2003 | DOI: 10.1034/j.1399-0004.2003.00036.x

  4. Short Reports

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor
    1. Two novel mutations in the α-galactosidase A gene in Chinese patients with Fabry disease (pages 205–209)

      C-C Yang, L-W Lai, O Whitehair, W-L Hwu, S-C Chiang and Y-HH Lien

      Version of Record online: 12 APR 2003 | DOI: 10.1034/j.1399-0004.2003.00050.x

    2. Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects (pages 210–214)

      E Rampersaud, EC Melvin, D Siegel, L Mehltretter, ME Dickerson, TM George, D Enterline, JS Nye, MC Speer and the NTD Collaborative Group

      Version of Record online: 12 APR 2003 | DOI: 10.1034/j.1399-0004.2003.00043.x

    3. Identification of a deletion in the mismatch repair gene, MSH2, using mouse–human cell hybrids monosomal for chromosome 2 (pages 215–218)

      RE Pyatt, H Nakagawa, H Hampel, M Sedra, MB Fuchik, I Comeras, A De La Chapelle and TW Prior

      Version of Record online: 12 APR 2003 | DOI: 10.1034/j.1399-0004.2003.00040.x

    4. Genetic control of serum IgE levels: a study of low molecular weight protein tyrosine phosphatase (pages 228–231)

      N Bottini, A Otsu, P Borgiani, P Saccucci, L Stefanini, E Greco, L Fontana, JM Hopkins and X-Q Mao

      Version of Record online: 12 APR 2003 | DOI: 10.1034/j.1399-0004.2003.00002.x

  5. Letters to the Editor

    1. Top of page
    2. Mini Review
    3. Hotspots
    4. Original Articles
    5. Short Reports
    6. Letters to the Editor

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