The origin and spread of the HFE-C282Y haemochromatosis mutation S. DistanteK. J. H. RobsonMark Worwood Review Article 29 July 2004 Pages: 269 - 279
Inheritance mode of multiple sclerosis: the effect of HLA class II alleles is stronger than additive Maartje BoonIlja M. NolteGerard J. te Meerman Original Investigation 05 August 2004 Pages: 280 - 284
Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters, SLC23A1 and SLC23A2 Peter EckHans Christian ErichsenStephen J. Chanock Original Investigation 14 August 2004 Pages: 285 - 294
Variations in the C3, C3a receptor, and C5 genes affect susceptibility to bronchial asthma Koichi HasegawaMayumi TamariYoichi Suzuki Original Investigation 27 July 2004 Pages: 295 - 301
CHX10 mutations cause non-syndromic microphthalmia/anophthalmia in Arab and Jewish kindreds Udy Bar-YosefIzzeldin AbuelaishOhad S. Birk Original Investigation 15 July 2004 Pages: 302 - 309
Association between evolutionary history of angiotensinogen haplotypes and plasma levels Laura FejermanNourdine BouzekriRichard S. Cooper Original Investigation 27 July 2004 Pages: 310 - 318
Genomic rearrangements at the IGHMBP2 gene locus in two patients with SMARD1 Ulf P. GuentherMarkus SchuelkeRaymonda Varon Original Investigation 29 July 2004 Pages: 319 - 326
Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array Xiaofeng ZhouSamuel C. MokDavid T. W. Wong Original Investigation 28 July 2004 Pages: 327 - 330
Gender- and age-specific contributions of additional DNA sequence variation in the 5′ regulatory region of the APOE gene to prediction of measures of lipid metabolism Ruth Frikke-SchmidtCharles F. SingAnne Tybjærg-Hansen Original Investigation 05 August 2004 Pages: 331 - 345
E.A. Carlson (ed) Mendel’s Legacy: the origin of classical genetics (2004) Peter S. Harper Book Review 14 July 2004 Pages: 346 - 346
