1. Association of genetic polymorphisms of alcohol-metabolizing enzymes with excessive alcohol consumption in Japanese men

   • F. Sun
   • I. Tsuritani
   • Y. Yamada

   Original Investigation 28 August 1999 Pages: 295 - 300

2. Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products

   • M. Goto
   • Y. Yamabe
   • Y. Furuichi

   Original Investigation 14 September 1999 Pages: 301 - 307

3. Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?

   • M. D’Alessandro
   • I. Naom
   • F. Muntoni

   Original Investigation 31 August 1999 Pages: 308 - 313

4. β3-Adrenergic receptor Trp64Arg polymorphism does not predict incident CHD or carotid intima-media thickness in a community-based sample of whites: the ARIC study

   • A.C. Morrison
   • F.L. Brancati
   • E. Boerwinkle

   Original Investigation 07 September 1999 Pages: 314 - 319

5. Characterisation of the human snail (SNAI1) gene and exclusion as a major disease gene in craniosynostosis

   • S.R.F. Twigg
   • A.O.M. Wilkie

   Original Investigation 08 September 1999 Pages: 320 - 326

6. Evaluation of the protein truncation test and mutation detection in the NF1 gene: mutational analysis of 15 known and 40 unknown mutations

   • M.J. Osborn
   • M. Upadhyaya

   Original Investigation 10 September 1999 Pages: 327 - 332

7. Long polymerase chain reaction in detection of germline deletions in the von Hippel-Lindau tumour suppressor gene

   • C. Cybulski
   • K. Krzystolik
   • J. Lubiński

   Original Investigation 09 September 1999 Pages: 333 - 336

8. CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genes

   • M. Clementi
   • P. Forabosco
   • R. Tenconi

   Original Investigation 07 September 1999 Pages: 337 - 342

9. G130V, a common FRDA point mutation, appears to have arisen from a common founder

   • M.B. Delatycki
   • M. Knight
   • S.M. Forrest

   Original Investigation 07 September 1999 Pages: 343 - 346

10. Chromosomal localization of three human poly(A)-binding protein genes and four related pseudogenes

    • C. Féral
    • M. G. Mattéi
    • G. Guellaën

    Original Investigation 15 September 1999 Pages: 347 - 353

11. Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor gene

    • K.R. Bowles
    • J. Gibson
    • N.E. Bowles

    Original Investigation 26 August 1999 Pages: 354 - 359

12. Influence of genotypes at SAA1 and SAA2 loci on the development and the length of latent period of secondary AA-amyloidosis in patients with rheumatoid arthritis

    • M. Moriguchi
    • C. Terai
    • N. Kamatani

    Original Investigation 14 September 1999 Pages: 360 - 366

13. X/Y translocation in a family with Leri-Weill dyschondrosteosis

    • G. Calabrese
    • R. Fischetto
    • G. Palka

    Short Report 25 August 1999 Pages: 367 - 368

14. Erratum to: Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases

    • Miguel Angel Pujana
    • Jordi Corral
    • Tha Ataxia Study Group

    Erratum 16 September 1999 Pages: 376 - 376

15. Erratum to: Intragenic polymorphic missense mutations in the XLRS1 gene in families with juvenile X-linked retinoschisis

    • Miki Hiraoka
    • Michael T. Trese
    • Barkur S. Shastry

    Erratum 16 September 1999 Pages: 377 - 377