Table of contents
January 2000 - Volume 37 - 1
Review article
- Friedreich ataxia: an overview (1 January, 2000)
Original articles
- Prevalent connexin 26 gene (GJB2) mutations in Japanese(1 January, 2000)
- A search for evidence of somatic mutations in theNF1 gene(1 January, 2000)
Short reports
- Cryptic subtelomeric translocations in the 22q13 deletion syndrome (1 January, 2000)
Letters to the editor
- A case of inv dup(8p) with early onset breast cancer (1 January, 2000)
- NF2gene deletion in a family with a mild phenotype(1 January, 2000)
- Absence of fragile X syndrome in Nova Scotia (1 January, 2000)