1. Identification of a novel type 1 diabetes susceptibility gene, T-bet

   • Yuka Sasaki
   • Kenji Ihara
   • Toshiro Hara

   Original Investigation 06 July 2004 Pages: 177 - 184

   

2. Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin gene

   • Sylvia L. Anderson
   • Josef Ekstein
   • Berish Y. Rubin

   Original Investigation 23 June 2004 Pages: 185 - 190

   

3. Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss

   • Gülistan Meşe
   • Eric Londin
   • Thomas W. White

   Original Investigation 07 July 2004 Pages: 191 - 199

   

4. Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis

   • Sahan V. Rannan-Eliya
   • Indira B. Taylor
   • Andrew O. M. Wilkie

   Original Investigation 07 July 2004 Pages: 200 - 207

   

5. A resistin gene polymorphism is associated with body mass index in women

   • Vanessa S. Mattevi
   • Verônica M. Zembrzuski
   • Mara H. Hutz

   Original Investigation 23 June 2004 Pages: 208 - 212

   

6. Mono-nucleotide repeats (MNRs): a neglected polymorphism for generating high density genetic maps in silico

   • Helit Cohen
   • Yael Danin-Poleg
   • Yechezkel Kashi

   Original Investigation 01 July 2004 Pages: 213 - 220

   

7. Directional migration in the Hindu castes: inferences from mitochondrial, autosomal and Y-chromosomal data

   • Stephen Wooding
   • Christopher Ostler
   • Lynn B. Jorde

   Original Investigation 01 July 2004 Pages: 221 - 229

   

8. Chromosome 17p12-q11 harbors susceptibility loci for systemic lupus erythematosus

   • Cecilia M. Johansson
   • Renata Zunec
   • Marta E. Alarcón-Riquelme

   Original Investigation 01 July 2004 Pages: 230 - 238

   

9. Qualitative and quantitative analysis of the effect of splicing mutations in propionic acidemia underlying non-severe phenotypes

   • Sonia Clavero
   • Belén Pérez
   • Lourdes R. Desviat

   Original Investigation 02 July 2004 Pages: 239 - 247

   

10. A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II

    • J.-W. Kim
    • S.-H. Nam
    • J. P. Simmer

    Original Investigation 06 July 2004 Pages: 248 - 254

    

11. Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage

    • Jianfeng Xu
    • Carl D. Langefeld
    • William B. Isaacs

    Original Investigation 05 June 2004 Pages: 255 - 262

    

12. Mutation analysis of subjects with 46, XX sex reversal and 46, XY gonadal dysgenesis does not support the involvement of SOX3 in testis determination

    • Han N. Lim
    • Gary D. Berkovitz
    • J. Ross Hawkins

    Erratum 09 July 2004 Pages: 263 - 263

13. B. Wissinger, S. Kohl, U. Langenbeck (eds): Developments in ophthalmology vol 37: Genetics in ophthalmology

    • G. C. M. Black

    Book Review 02 July 2004 Pages: 264 - 264

14. Alan E. Guttmacher, Francis S. Collins, Jeffrey M. Drazen (eds): Genomic medicine: articles from the New England Journal of Medicine

    • Andrew P. Read

    Book Review 16 June 2004 Pages: 265 - 266

15. Max Perutz (ed) I wish I’d make you angry earlier. Expanded edition (2003)

    • Peter S. Harper

    Book Review 02 July 2004 Pages: 267 - 267

16. Thomas von Zglinicki (ed) Aging at the molecular level (2003)

    • Holger Hoehn

    Book Review 02 July 2004 Pages: 268 - 268