Association of genetic polymorphisms of alcohol-metabolizing enzymes with excessive alcohol consumption in Japanese men F. SunI. TsuritaniY. Yamada Original Investigation 28 August 1999 Pages: 295 - 300
Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products M. GotoY. YamabeY. Furuichi Original Investigation 14 September 1999 Pages: 301 - 307
Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy? M. D’AlessandroI. NaomF. Muntoni Original Investigation 31 August 1999 Pages: 308 - 313
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. MorrisonF.L. BrancatiE. Boerwinkle Original Investigation 07 September 1999 Pages: 314 - 319
Characterisation of the human snail (SNAI1) gene and exclusion as a major disease gene in craniosynostosis S.R.F. TwiggA.O.M. Wilkie Original Investigation 08 September 1999 Pages: 320 - 326
Evaluation of the protein truncation test and mutation detection in the NF1 gene: mutational analysis of 15 known and 40 unknown mutations M.J. OsbornM. Upadhyaya Original Investigation 10 September 1999 Pages: 327 - 332
Long polymerase chain reaction in detection of germline deletions in the von Hippel-Lindau tumour suppressor gene C. CybulskiK. KrzystolikJ. Lubiński Original Investigation 09 September 1999 Pages: 333 - 336
CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genes M. ClementiP. ForaboscoR. Tenconi Original Investigation 07 September 1999 Pages: 337 - 342
G130V, a common FRDA point mutation, appears to have arisen from a common founder M.B. DelatyckiM. KnightS.M. Forrest Original Investigation 07 September 1999 Pages: 343 - 346
Chromosomal localization of three human poly(A)-binding protein genes and four related pseudogenes C. FéralM. G. MattéiG. Guellaën Original Investigation 15 September 1999 Pages: 347 - 353
Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor gene K.R. BowlesJ. GibsonN.E. Bowles Original Investigation 26 August 1999 Pages: 354 - 359
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. MoriguchiC. TeraiN. Kamatani Original Investigation 14 September 1999 Pages: 360 - 366
X/Y translocation in a family with Leri-Weill dyschondrosteosis G. CalabreseR. FischettoG. Palka Short Report 25 August 1999 Pages: 367 - 368
Erratum to: Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases Miguel Angel PujanaJordi CorralTha Ataxia Study Group Erratum 16 September 1999 Pages: 376 - 376
Erratum to: Intragenic polymorphic missense mutations in the XLRS1 gene in families with juvenile X-linked retinoschisis Miki HiraokaMichael T. TreseBarkur S. Shastry Erratum 16 September 1999 Pages: 377 - 377