1. A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease

   • Jian-Min Chen
   • Peter D. Stenson
   • Claude Férec

   Review Article 28 June 2005 Pages: 411 - 427

   

2. Significant genetic differentiation between Poland and Germany follows present-day political borders, as revealed by Y-chromosome analysis

   • Manfred Kayser
   • Oscar Lao
   • Rafal Ploski

   Original Investigation 16 June 2005 Pages: 428 - 443

   

3. Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides

   • Hilary Coon
   • Yuanpei Xin
   • Steven C. Hunt

   Original Investigation 16 June 2005 Pages: 444 - 451

4. Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations

   • Tim Forshew
   • Colin A. Johnson
   • Eamonn R. Maher

   Original Investigation 16 June 2005 Pages: 452 - 459

   

5. A homozygous COL6A2 intron mutation causes in-frame triple-helical deletion and nonsense-mediated mRNA decay in a patient with Ullrich congenital muscular dystrophy

   • Laura Lucarini
   • Betti Giusti
   • Mon-Li Chu

   Original Investigation 17 June 2005 Pages: 460 - 466

   

6. The Q283P amino-acid change in HFE leads to structural and functional consequences similar to those described for the mutated 282Y HFE protein

   • Chandran Ka
   • Gérald Le Gac
   • Claude Férec

   Original Investigation 18 June 2005 Pages: 467 - 475

   

7. Intercellular adhesion molecule-1 and childhood asthma

   • Yu-Fen Li
   • Yo-Hsuang Tsao
   • Frank D. Gilliland

   Original Investigation 14 July 2005 Pages: 476 - 484

   

8. DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein–Taybi syndrome (RSTS) and in another patient with incomplete RSTS

   • Oliver Bartsch
   • Stefanie Schmidt
   • Sasan Rasi

   Original Investigation 14 July 2005 Pages: 485 - 493

   

9. Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia

   • France Gagnon
   • Gail P. Jarvik
   • Ellen M. Wijsman

   Original Investigation 16 June 2005 Pages: 494 - 505

   

10. Silvia Garagna (ed) Mouse genetics after the mouse genome. Karger, ISBN 3-805-57783-4, hardcover

    • Steve D. M. Brown

    Book Review 23 June 2005 Pages: 506 - 507

11. Yury Verlinsky and Anver Kuliev (eds) Atlas of preimplantation genetic diagnosis, 2nd edition. Taylor & Francis, ISBN 1-842-14245-3, hardcover

    • Frances Flinter

    Book Review 28 June 2005 Pages: 508 - 508

12. Human Molecular Genetics, 3rd edition, by Tom Strachan, Andrew Read. Garland Science, ISBN 0-8153-4184-9, paperback

    • Xavier Estivill

    Book Review 29 June 2005 Pages: 509 - 509