1. Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion

   • Morten Dunø
   • Hanne Hove
   • Marianne Schwartz

   Original Investigation 18 September 2004 Pages: 459 - 467

   

2. Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study

   • Donna K. Arnett
   • Michael B. Miller
   • John H. Eckfeldt

   Original Investigation 16 September 2004 Pages: 468 - 474

   

3. The human T locus and spina bifida risk

   • Liselotte E. Jensen
   • Sandrine Barbaux
   • Laura E. Mitchell

   Original Investigation 24 September 2004 Pages: 475 - 482

   

4. The CLCA gene locus as a modulator of the gastrointestinal basic defect in cystic fibrosis

   • Margit Ritzka
   • Frauke Stanke
   • Burkhard Tümmler

   Original Investigation 13 October 2004 Pages: 483 - 491

   

5. Y chromosome haplogroups of elite Ethiopian endurance runners

   • Colin N. Moran
   • Robert A. Scott
   • Yannis P. Pitsiladis

   Original Investigation 20 October 2004 Pages: 492 - 497

   

6. Mutational analysis of OGG1, MYH, MTH1 in FAP, HNPCC and sporadic colorectal cancer patients: R154H OGG1 polymorphism is associated with sporadic colorectal cancer patients

   • I.-J. Kim
   • J.-L. Ku
   • J.-G. Park

   Original Investigation 24 September 2004 Pages: 498 - 503

   

7. Diet and the frequency of the alanine:glyoxylate aminotransferase Pro11Leu polymorphism in different human populations

   • Elizabeth F. Caldwell
   • Lianne R. Mayor
   • Christopher J. Danpure

   Original Investigation 05 October 2004 Pages: 504 - 509

   

8. FISH diagnosis of the common 57-kb deletion in CTNS causing cystinosis

   • Claude Bendavid
   • Robert Kleta
   • William A. Gahl

   Original Investigation 09 September 2004 Pages: 510 - 514

   

9. Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome

   • Weimin Bi
   • G. Mustafa Saifi
   • James R. Lupski

   Original Investigation 30 September 2004 Pages: 515 - 524

   

10. Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome

    • Yoshihiro Maruo
    • Carlos D′ Addario
    • Yoshihiro Takeuchi

    Short Report 17 September 2004 Pages: 525 - 526

11. Francis Galton: Pioneer of heredity and biometry (2003)

    • R. J. Berry

    Book Review 18 September 2004 Pages: 527 - 528

12. Emery A.E.H., Muntoni F. (eds): Duchenne muscular dystrophy.

    • Clemens R. Mueller

    Book Review 25 September 2004 Pages: 529 - 529

13. TP53 haplotype-based analysis and incidence of post-angioplasty restenosis

    • Robert Y. L. Zee
    • Nancy R. Cook
    • Klaus Lindpaintner

    Erratum 13 October 2004 Pages: 530 - 530

14. Mutations

    Human Gene Mutations 24 November 2004 Pages: 531 - 534