Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population Dolores Garcia ArocenaKatherine E. BreecePaul J. Hagerman Original Investigation 07 August 2003 Pages: 371 - 376
Association of a promoter variant in the inducible cyclooxygenase-2 gene (PTGS2) with type 2 diabetes mellitus in Pima Indians Yasmine L. KonheimJohanna K. Wolford Original Investigation 14 August 2003 Pages: 377 - 381
Novel mutations in the IRF6 gene for Van der Woude syndrome Xiaofang WangJiali LiuXiangyin Kong Original Investigation 14 August 2003 Pages: 382 - 386
A common IL-13 Arg130Gln single nucleotide polymorphism among Chinese atopy patients with allergic rhinitis Min WangZhi-Min XingLi-Sheng Yu Original Investigation 20 August 2003 Pages: 387 - 390
Mitochondrial DNA sequence polymorphisms of five ethnic populations from northern China Qing-Peng KongYong-Gang YaoYa-Ping Zhang Original Investigation 21 August 2003 Pages: 391 - 405
Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin Robert GrabskiTomasz SzulElizabeth Sztul Original Investigation 20 August 2003 Pages: 406 - 416
Molecular variation at the apolipoprotein B gene locus in relation to lipids and cardiovascular disease: a systematic meta-analysis S. Matthijs BoekholdtRon J. G. PetersEric J. G. Sijbrands Original Investigation 26 August 2003 Pages: 417 - 425
Functional analysis of intra-allelic variation at NACP-Rep1 in the α-synuclein gene Ornit Chiba-FalekJeffrey W. TouchmanRobert L. Nussbaum Original Investigation 16 August 2003 Pages: 426 - 431
Association of the mitochondrial DNA 15497G/A polymorphism with obesity in a middle-aged and elderly Japanese population Tomohiro OkuraMichiko KodaHiroshi Shimokata Original Investigation 02 August 2003 Pages: 432 - 436
Sex differences in heritability of sensitization to Blomia tropicalis in asthma using regression of offspring on midparent (ROMP) methods Teri A. ManolioKathleen C. BarnesAlexander F. Wilson Original Investigation 20 August 2003 Pages: 437 - 446
Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12) V. Reid SuttonWilliam H. McAlisterAngela J. Villar Original Investigation 21 August 2003 Pages: 447 - 451
Inherited BRCA2 mutations in African Americans with breast and/or ovarian cancer: a study of familial and early onset cases Yasmine KanaanElikem KpenuCarolyn Broome Original Investigation 26 August 2003 Pages: 452 - 460
Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy in a South Indian population J. VijaiA. KapoorA. Anand Short Report 20 August 2003 Pages: 461 - 463
Nicholas T. Potter (editor) Methods in molecular biology, volume 217. Neurogenetics: methods and protocols Mary B. Davis Book Review 02 August 2003 Pages: 464 - 464