1. Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population

   • Dolores Garcia Arocena
   • Katherine E. Breece
   • Paul J. Hagerman

   Original Investigation 07 August 2003 Pages: 371 - 376

   

2. Association of a promoter variant in the inducible cyclooxygenase-2 gene (PTGS2) with type 2 diabetes mellitus in Pima Indians

   • Yasmine L. Konheim
   • Johanna K. Wolford

   Original Investigation 14 August 2003 Pages: 377 - 381

3. Novel mutations in the IRF6 gene for Van der Woude syndrome

   • Xiaofang Wang
   • Jiali Liu
   • Xiangyin Kong

   Original Investigation 14 August 2003 Pages: 382 - 386

   

4. A common IL-13 Arg130Gln single nucleotide polymorphism among Chinese atopy patients with allergic rhinitis

   • Min Wang
   • Zhi-Min Xing
   • Li-Sheng Yu

   Original Investigation 20 August 2003 Pages: 387 - 390

5. Mitochondrial DNA sequence polymorphisms of five ethnic populations from northern China

   • Qing-Peng Kong
   • Yong-Gang Yao
   • Ya-Ping Zhang

   Original Investigation 21 August 2003 Pages: 391 - 405

   

6. Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin

   • Robert Grabski
   • Tomasz Szul
   • Elizabeth Sztul

   Original Investigation 20 August 2003 Pages: 406 - 416

   

7. Molecular variation at the apolipoprotein B gene locus in relation to lipids and cardiovascular disease: a systematic meta-analysis

   • S. Matthijs Boekholdt
   • Ron J. G. Peters
   • Eric J. G. Sijbrands

   Original Investigation 26 August 2003 Pages: 417 - 425

   

8. Functional analysis of intra-allelic variation at NACP-Rep1 in the α-synuclein gene

   • Ornit Chiba-Falek
   • Jeffrey W. Touchman
   • Robert L. Nussbaum

   Original Investigation 16 August 2003 Pages: 426 - 431

   

9. Association of the mitochondrial DNA 15497G/A polymorphism with obesity in a middle-aged and elderly Japanese population

   • Tomohiro Okura
   • Michiko Koda
   • Hiroshi Shimokata

   Original Investigation 02 August 2003 Pages: 432 - 436

10. Sex differences in heritability of sensitization to Blomia tropicalis in asthma using regression of offspring on midparent (ROMP) methods

    • Teri A. Manolio
    • Kathleen C. Barnes
    • Alexander F. Wilson

    Original Investigation 20 August 2003 Pages: 437 - 446

    

11. Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12)

    • V. Reid Sutton
    • William H. McAlister
    • Angela J. Villar

    Original Investigation 21 August 2003 Pages: 447 - 451

    

12. Inherited BRCA2 mutations in African Americans with breast and/or ovarian cancer: a study of familial and early onset cases

    • Yasmine Kanaan
    • Elikem Kpenu
    • Carolyn Broome

    Original Investigation 26 August 2003 Pages: 452 - 460

    

13. Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy in a South Indian population

    • J. Vijai
    • A. Kapoor
    • A. Anand

    Short Report 20 August 2003 Pages: 461 - 463

14. 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

15. Mutations

    Human Gene Mutations 12 September 2003 Pages: 465 - 465