1. Update on the genetics of migraine

   • Miguel Estevez
   • Kathy L. Gardner

   Review Article 18 November 2003 Pages: 225 - 235

   

2. Analysis of heat-shock protein 70 gene polymorphisms and the risk of Parkinson’s disease

   • Yih-Ru Wu
   • Cheng-Kuang Wang
   • Guey-Jen Lee-Chen

   Original Investigation 06 November 2003 Pages: 236 - 241

   

3. A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia

   • Dolrudee Jumlongras
   • Jenn-Yih Lin
   • Bjorn R. Olsen

   Original Investigation 19 December 2003 Pages: 242 - 249

   

4. Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysm

   • James M. Farnham
   • Nicola J. Camp
   • Lisa A. Cannon-Albright

   Original Investigation 06 November 2003 Pages: 250 - 255

   

5. Modulation of penetrance by the wild-type allele in dominantly inherited erythropoietic protoporphyria and acute hepatic porphyrias

   • Laurent Gouya
   • Hervé Puy
   • Jean-Charles Deybach

   Original Investigation 11 December 2003 Pages: 256 - 262

   

6. Mexican American ancestry-informative markers: examination of population structure and marker characteristics in European Americans, Mexican Americans, Amerindians and Asians

   • Heather E. Collins-Schramm
   • Bill Chima
   • Michael F. Seldin

   Original Investigation 20 November 2003 Pages: 263 - 271

   

7. Haplotype mapping of the bronchiolitis susceptibility locus near IL8

   • Jeremy Hull
   • Kate Rowlands
   • Dominic P. Kwiatkowski

   Original Investigation 06 November 2003 Pages: 272 - 279

   

8. Apolipoprotein B-100 XbaI gene polymorphism in gallbladder cancer

   • Mahendra Kumar Singh
   • Udai Bhan Pandey
   • Balraj Mittal

   Original Investigation 14 November 2003 Pages: 280 - 283

9. Genetic and clinical mosaicism in a patient with neurofibromatosis type 1

   • Ina Vandenbroucke
   • Remco van Doorn
   • Ludwine Messiaen

   Original Investigation 06 November 2003 Pages: 284 - 290

   

10. Localized aggressive periodontitis is linked to human chromosome 1q25

    • Yefu Li
    • Lin Xu
    • Thomas E. Van Dyke

    Original Investigation 12 December 2003 Pages: 291 - 297

    

11. Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28

    • Nadine Gigarel
    • Nelly Frydman
    • Pierre F. Ray

    Original Investigation 12 December 2003 Pages: 298 - 305

    

12. Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy

    • Anna Kaminska
    • Sergei V. Strelkov
    • Lev G. Goldfarb

    Original Investigation 27 November 2003 Pages: 306 - 313

    

13. Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria

    • Joaquim Calado
    • Karina Soto
    • José Rueff

    Short Report 12 November 2003 Pages: 314 - 316

    

14. Bronya J.B. Keats, Arthur N. Popper, Richard R. Fay (Editors) Springer handbook of auditory research: genetics and auditory disorders

    • Richard C. Trembath

    Book Review 11 December 2003 Pages: 317 - 317

15. Genetics and genomics of neurobehavioral disorders

    • Randi J. Hagerman

    Book Review 11 December 2003 Pages: 318 - 319

16. G. Bates, P. Harper, L. Jones (eds): Huntington’s Disease, Third Edition

    • Allan J. Tobin

    Book Review 09 December 2003 Pages: 320 - 321

17. Members of the CDY family have different expression patterns: CDY1 transcripts have the best correlation with complete spermatogenesis

    • Sandra E. Kleiman
    • Leah Yogev
    • Haim Yavetz

    Erratum 12 December 2003 Pages: 322 - 322

    

18. Acknowledgement to referees 2003

    Acknowledgement to Referees 23 January 2004 Pages: 323 - 325

19. Public Health Genetics

    Announcements 23 January 2004 Pages: 326 - 326