1. Parents of children with autosomal recessive diseases are not always carriers of the respective mutant alleles

   • Joel Zlotogora

   Review Article 16 March 2004 Pages: 521 - 526

2. A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24

   • Bei-sha Tang
   • Wei Luo
   • Oleg V. Evgrafov

   Original Investigation 12 March 2004 Pages: 527 - 533

   

3. Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene

   • Joanne E. Langan
   • Charlotte G. Cole
   • Janet M. Risk

   Original Investigation 09 March 2004 Pages: 534 - 540

   

4. Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing

   • Jennifer Winter
   • Tanja Lehmann
   • Susann Schweiger

   Original Investigation 31 March 2004 Pages: 541 - 552

   

5. SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome

   • Maren Runte
   • Peter M. Kroisel
   • Karin Buiting

   Original Investigation 10 March 2004 Pages: 553 - 561

   

6. Fine mapping a gene for pediatric gastroesophageal reflux on human chromosome 13q14

   • Fen Ze Hu
   • Joseph Donfack
   • Robert A. Preston

   Original Investigation 10 March 2004 Pages: 562 - 572

7. Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis

   • Justin P. Rubio
   • Melanie Bahlo
   • Trevor J. Kilpatrick

   Original Investigation 11 March 2004 Pages: 573 - 580

   

8. Variants of CYP46A1 may interact with age and APOE to influence CSF Aβ42 levels in Alzheimer’s disease

   • Annica Johansson
   • Hagit Katzov
   • Jonathan A. Prince

   Original Investigation 18 March 2004 Pages: 581 - 587

9. Quasi-linkage: a confounding factor in linkage analysis of complex diseases?

   • Sinthuja Sivagnanasundaram
   • Karl W. Broman
   • Arturas Petronis

   Original Investigation 26 March 2004 Pages: 588 - 593

10. Fine mapping of the Schnyder’s crystalline corneal dystrophy locus

    • Veena Theendakara
    • Gerard Tromp
    • Jayne S. Weiss

    Original Investigation 19 March 2004 Pages: 594 - 600

    

11. Microarray Gene Expression Data Analysis: A Beginners Guide

    • Lesley Jones
    • Gareth Hughes

    Book Review 23 March 2004 Pages: 601 - 602

12. The Genetic Basis of Common Diseases, 2nd Edition

    • Andrew Green

    Book Review 19 March 2004 Pages: 603 - 604

13. Genetics of Movement Disorders

    • Anne Rosser

    Book Review 23 March 2004 Pages: 605 - 605

14. Mutations

    Human Gene Mutations 22 April 2004 Pages: 606 - 609