1. Genetics of parkin-linked disease

   • Andrew B. West
   • Nigel T. Maidment

   Review 15 January 2004 Pages: 327 - 336

   

2. Leukotriene-related gene polymorphisms in ASA-intolerant asthma: an association with a haplotype of 5-lipoxygenase

   • Jeong-Hee Choi
   • Hae-Sim Park
   • Hyoung-Doo Shin

   Original Investigation 29 January 2004 Pages: 337 - 344

3. Novel SBDS mutations caused by gene conversion in Japanese patients with Shwachman-Diamond syndrome

   • Eiji Nakashima
   • Akihiko Mabuchi
   • Shiro Ikegawa

   Original Investigation 29 January 2004 Pages: 345 - 348

   

4. A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree

   • Kirsten M. Timms
   • Susanne Wagner
   • Donna M. Shattuck

   Original Investigation 15 January 2004 Pages: 349 - 353

   

5. Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations

   • Doron M. Behar
   • Daniel Garrigan
   • Michael F. Hammer

   Original Investigation 22 January 2004 Pages: 354 - 365

   

6. Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis

   • Amos Frisch
   • Roberto Colombo
   • Leah Peleg

   Original Investigation 15 January 2004 Pages: 366 - 376

   

7. Patterns of linkage disequilibrium in the MHC region on human chromosome 6p

   • Annette Stenzel
   • Timothy Lu
   • Stefan Schreiber

   Original Investigation 22 January 2004 Pages: 377 - 385

   

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

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

   Original Investigation 22 January 2004 Pages: 386 - 390

9. Common variants within the interleukin 4 receptor α gene (IL4R) are associated with susceptibility to osteoarthritis

   • Tracy Forster
   • Kay Chapman
   • John Loughlin

   Original Investigation 24 January 2004 Pages: 391 - 395

10. The assertion that a G21V mutation in AGTR2 causes mental retardation is not supported by other studies

    • Jeanette Erdmann
    • Steffen Dähmlow
    • Vera Regitz-Zagrosek

    Letter to the Editors 13 January 2004 Pages: 396 - 396

11. AGTR2 mutation and mental retardation: a reply

    • Tero Ylisaukko-oja
    • Irma Järvelä

    Letter to the Editors 13 January 2004 Pages: 397 - 397

12. U. Eiholzer, D. L’Allemand, WB. Zipf (eds): Prader-Willi syndrome as a model for obesity

    • Jill Clayton-Smith

    Book Review 15 January 2004 Pages: 398 - 398

13. David Reiss, Jenae M. Neiderhiser, E. Mavis Hetherington, Robert Plomin (Editors): The relationship code: deciphering genetic and social influences on adolescent development

    • Frances Rice

    Book Review 13 January 2004 Pages: 399 - 399

14. R. Horowoski, Y. Mizuno, C.W. Olanow, W.H. Poewe, P. Riederer, J.A. Stoessl, M.B.H. Youdim (Editors) Advances in research on neurodegeneration (volume 10)

    • Roger Barker

    Book Review 13 January 2004 Pages: 400 - 400

15. Nucleotide and haplotypic diversity of the NOS2A promoter region and its relationship to cerebral malaria

    • David Burgner
    • Stanley Usen
    • Dominic P. Kwiatkowski

    Erratum 20 January 2004 Pages: 401 - 401

16. Mutations

    Human Gene Mutations 24 February 2004 Pages: 402 - 411