1. The neurobeachin gene spans the common fragile site FRA13A

   • Larissa Savelyeva
   • Evgeny Sagulenko
   • Manfred Schwab

   Original Investigation 22 October 2005 Pages: 551 - 558

   

2. Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy

   • Sarah A. Shoichet
   • Laurence Duprez
   • Vera M. Kalscheuer

   Original Investigation 25 October 2005 Pages: 559 - 567

   

3. Variation in genes involved in the RANKL/RANK/OPG bone remodeling pathway are associated with bone mineral density at different skeletal sites in men

   • Yi-Hsiang Hsu
   • Tianhua Niu
   • Xiping Xu

   Original Investigations 26 October 2005 Pages: 568 - 577

   

4. Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation

   • Olivier Hagens
   • Aline Dubos
   • André Hanauer

   Original Investigation 26 October 2005 Pages: 578 - 590

   

5. Contrasting patterns of Y-chromosome variation in South Siberian populations from Baikal and Altai-Sayan regions

   • Miroslava Derenko
   • Boris Malyarchuk
   • Ilia Zakharov

   Original Investigation 27 October 2005 Pages: 591 - 604

   

6. A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3

   • Muhammad Jawad Hassan
   • Regie Lyn P. Santos
   • Suzanne M. Leal

   Original Investigation 29 October 2005 Pages: 605 - 610

   

7. Ring chromosome 15: characterization by array CGH

   • Ian A. Glass
   • Katherine A. Rauen
   • Philip D. Cotter

   Original Investigation 03 November 2005 Pages: 611 - 617

   

8. Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation

   • Liesbet Deprez
   • Lieve R. F. Claes
   • Peter De Jonghe

   Original Investigation 05 November 2005 Pages: 618 - 625

   

9. Admixture-matched case-control study: a practical approach for genetic association studies in admixed populations

   • Hui-Ju Tsai
   • Jennifer Y. Kho
   • Esteban González Burchard

   Original Investigation 05 November 2005 Pages: 626 - 639

   

10. A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions

    • K. L. Lachlan
    • S. Youings
    • N. S. Thomas

    Original Investigation 08 November 2005 Pages: 640 - 651

    

11. Population stratification confounds genetic association studies among Latinos

    • Shweta Choudhry
    • Natasha E. Coyle
    • Genetics of Asthma in Latino Americans (GALA) Study

    Original Investigation 08 November 2005 Pages: 652 - 664

    

12. Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33–q27.3

    • Peter John
    • Ghazanfar Ali
    • Wasim Ahmad

    Short Report 05 November 2005 Pages: 665 - 667

    

13. Molecular analysis of a constitutional complex genome rearrangement with 11 breakpoints involving chromosomes 3, 11, 12, and 21 and a ∼0.5-Mb submicroscopic deletion in a patient with mild mental retardation

    • Katarzyna Borg
    • Paweł Stankiewicz
    • Tadeusz Mazurczak

    Erratum 23 November 2005 Pages: 668 - 668