1. GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation

   • Akihiro Ohtsuka
   • Isamu Yuge
   • Shin-ichi Usami

   Original Investigation 31 January 2003 Pages: 329 - 333

   

2. Biallelic expression of HRAS and MUCDHL in human and mouse

   • Michael Goldberg
   • Michelle Wei
   • Benjamin Tycko

   Original Investigation 14 February 2003 Pages: 334 - 342

   

3. Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin

   • K. Miller
   • B. Pabst
   • M. Arslan-Kirchner

   Original Investigation 06 February 2003 Pages: 343 - 347

   

4. Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese families

   • Norimoto Kobayashi
   • Kazunaga Agematsu
   • Atsushi Komiyama

   Original Investigation 19 February 2003 Pages: 348 - 352

   

5. High level of male-biased Scandinavian admixture in Greenlandic Inuit shown by Y-chromosomal analysis

   • Elena Bosch
   • Francesc Calafell
   • Mark A. Jobling

   Original Investigation 20 February 2003 Pages: 353 - 363

   

6. Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia

   • Ljubica Caldovic
   • Hiroki Morizono
   • Mendel Tuchman

   Original Investigation 20 February 2003 Pages: 364 - 368

   

7. Linkage of autosomal dominant common variable immunodeficiency to chromosome 5p and evidence for locus heterogeneity

   • D. U. Braig
   • A. A. Schäffer
   • B. Grimbacher

   Original Investigation 06 February 2003 Pages: 369 - 378

   

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

   • David Burgner
   • Stanley Usen
   • Dominic P. Kwiatkowski

   Original Investigation 28 January 2003 Pages: 379 - 386

   

9. Skin pigmentation, biogeographical ancestry and admixture mapping

   • Mark D. Shriver
   • Esteban J. Parra
   • Rick A. Kittles

   Original Investigation 11 February 2003 Pages: 387 - 399

   

10. Notch4, a non-HLA gene in the MHC is strongly associated with the most severe form of alopecia areata

    • R. Tazi-Ahnini
    • M. J. Cork
    • A. J. G. McDonagh

    Original Investigation 14 February 2003 Pages: 400 - 403

11. Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH)

    • Jian Wang
    • Robert A. Hegele

    Original Investigation 06 February 2003 Pages: 404 - 408

    

12. The interleukin-6 (−174) G/C promoter polymorphism is associated with type-2 diabetes mellitus in Native Americans and Caucasians

    • Barbora Vozarova
    • José-Manuel Fernández-Real
    • Johanna K. Wolford

    Original Investigation 14 February 2003 Pages: 409 - 413

13. Linkage analysis of prostate cancer susceptibility: confirmation of linkage at 8p22–23

    • Fredrik Wiklund
    • Björn-Anders Jonsson
    • Henrik Grönberg

    Original Investigation 20 February 2003 Pages: 414 - 418

    

14. An Alu-mediated rearrangement as cause of exon skipping in Hunter disease

    • Verena Ricci
    • Stefano Regis
    • Mirella Filocamo

    Original Investigation 11 February 2003 Pages: 419 - 425

    

15. Gene rearrangements in the glucocerebrosidase-metaxin region giving rise to disease-causing mutations and polymorphisms. Analysis of 25 RecNciI alleles in Gaucher disease patients

    • Anna Díaz-Font
    • Bru Cormand
    • Lluïsa Vilageliu

    Short Report 14 February 2003 Pages: 426 - 429

    

16. The signature motif in human glucose-6-phosphate transporter is essential for microsomal transport of glucose-6-phosphate

    • Chi-Jiunn Pan
    • Li-Yuan Chen
    • Janice Yang Chou

    Short Report 31 January 2003 Pages: 430 - 433

    

17. The future of association studies of common cancers

    • Richard S. Houlston
    • Julian Peto

    Letter to the Editors 06 February 2003 Pages: 434 - 435

    

18. Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter

    • Jens J. Hansen
    • Peter Bross
    • Niels Gregersen

    Erratum Pages: 436 - 436

19. Mutation analysis of the coding sequence of the MECP2 gene in infantile autism

    • Kim S. Beyer
    • Francesca Blasi
    •   International Molecular Genetic Study of Autism Consortium (IMGSAC)

    Erratum Pages: 437 - 437

20. C.W.R.J. Cremers, R.J.H. Smith (eds): Genetic hearing impairment—it's clinical presentations. Advances in Oto-Rhino-Laryngology, Vol 61 (Series ed: W. Arnold)

    • William Reardon

    Book Review 20 February 2003 Pages: 438 - 438

21. Structural and molecular basis of skeletal muscle diseases

    • Manuela C. Koch

    Book Review 20 February 2003 Pages: 439 - 439