1. Human hereditary hearing impairment: mouse models can help to solve the puzzle

   • Karen Vrijens
   • Lut Van Laer
   • Guy Van Camp

   Review Article 11 September 2008 Pages: 325 - 348

   

2. Osteoporosis: an evolutionary perspective

   • David Karasik

   Review Article 10 September 2008 Pages: 349 - 356

   

3. Identifying modifier genes of monogenic disease: strategies and difficulties

   • Emmanuelle Génin
   • Josué Feingold
   • Françoise Clerget-Darpoux

   Review article 11 September 2008 Pages: 357 - 368

   

4. The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis

   • Meltem Muftuoglu
   • Junko Oshima
   • Vilhelm A. Bohr

   Review Article 23 September 2008 Pages: 369 - 377

   

5. Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci

   • Kathryn P. Burdon
   • Douglas J. Coster
   • Jamie E. Craig

   Original Investigation 05 September 2008 Pages: 379 - 386

   

6. Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation

   • Acácia Fernandes Lacerda de Carvalho
   • Fernanda Teixeira da Silva Bellucco
   • Maria Isabel Melaragno

   Original Investigation 07 September 2008 Pages: 387 - 392

   

7. Association of amyloid precursor protein-binding protein, family B, member 1 with nicotine dependence in African and European American smokers

   • Guo-Bo Chen
   • Thomas J. Payne
   • Ming D. Li

   Original Investigation 07 September 2008 Pages: 393 - 398

   

8. Partial AZFc deletions and duplications: clinical correlates in the Italian population

   • Claudia Giachini
   • Ilaria Laface
   • Csilla Krausz

   Original Investigation 21 September 2008 Pages: 399 - 410

   

9. Association between Apolipoprotein E genotype and cerebral palsy is not confirmed in a Caucasian population

   • Gai L. McMichael
   • Catherine S. Gibson
   • for the South Australian Cerebral Palsy Research Group

   Original Investigation 23 September 2008 Pages: 411 - 416

10. Re-creation of the genetic composition of a founder population

    • William Klitz
    • Martin Maiers
    • Loren Gragert

    Original Investigation Open access 27 September 2008 Pages: 417 - 421

    

11. A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2–q26.33

    • Xiao-Hua Dai
    • Wen-Wu Chen
    • Jing-Yu Liu

    Original Investigation 02 October 2008 Pages: 423 - 429

    

12. Association of SIRT1 gene variation with visceral obesity

    • Armand V. Peeters
    • Sigri Beckers
    • Luc F. Van Gaal

    Original Investigation 27 September 2008 Pages: 431 - 436

13. Elof Axel Carlson: Neither gods nor beasts. How science is changing who we think we are

    • Caroline Berry

    Book Review 23 September 2008 Pages: 437 - 438