1. Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes

   • Gloria Ribas
   • Anna González-Neira
   • Javier Benítez

   Review Article 02 December 2005 Pages: 669 - 679

   

2. Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3A>G mutation that causes exon skipping

   • Pia Pinholt Madsen
   • Maria Kibæk
   • Brage Storstein Andresen

   Original Investigation 30 November 2005 Pages: 680 - 690

   

3. Extreme skewing of X chromosome inactivation in mothers of homosexual men

   • Sven Bocklandt
   • Steve Horvath
   • Dean H. Hamer

   Original Investigation 21 December 2005 Pages: 691 - 694

   

4. Phylogenetic relationship of the populations within and around Japan using 105 short tandem repeat polymorphic loci

   • Shi-Lin Li
   • Toshimichi Yamamoto
   • Naruya Saitou

   Original Investigation 29 November 2005 Pages: 695 - 707

   

5. SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

   • Masoud Garshasbi
   • Mohammad Mahdi Motazacker
   • Hossein Najmabadi

   Original Investigation 26 November 2005 Pages: 708 - 715

   

6. Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect

   • Bao-Li Chang
   • Ethan M. Lange
   • Jianfeng Xu

   Original Investigations 23 November 2005 Pages: 716 - 724

   

7. Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q

   • Alejandro A. Schäffer
   • Jessica Pfannstiel
   • Bodo Grimbacher

   Original Investigation 22 November 2005 Pages: 725 - 729

8. Variants in Deleted in AZoospermia-Like (DAZL) are correlated with reproductive parameters in men and women

   • Joyce Y. Tung
   • Mitchell P. Rosen
   • Renee A. Reijo Pera

   Original Investigation 22 November 2005 Pages: 730 - 740

   

9. Human F7 sequence is split into three deep clades that are related to FVII plasma levels

   • Maria Sabater-Lleal
   • José Manuel Soria
   • Francesc Calafell

   Original Investigation 16 November 2005 Pages: 741 - 751

   

10. Variants of the SFTPA1 and SFTPA2 genes and susceptibility to tuberculosis in Ethiopia

    • S. Malik
    • C.M.T. Greenwood
    • E. Schurr

    Original Investigation 15 November 2005 Pages: 752 - 759

    

11. The euchromatic 9p+ polymorphism is a locus-specific amplification caused by repeated copies of a small DNA segment mapping within 9p12

    • Rosetta Lecce
    • Marina Murdolo
    • Marcella Zollino

    Original Investigation 02 December 2005 Pages: 760 - 766

    

12. Activation of cryptic splice sites is a frequent splicing defect mechanism caused by mutations in exon and intron sequences of the OPA1 gene

    • Simone Schimpf
    • Simone Schaich
    • Bernd Wissinger

    Short Report 02 December 2005 Pages: 767 - 771

    

13. First steps in antenatal diagnosis, 1956

    • Povl Riis

    Historical & Personal Perspectives 14 December 2005 Pages: 772 - 773

14. Novel human pathological mutations 

    • Paul D. Lewis

    Human Gene Mutations 06 January 2006 Pages: 774 - 785

15. Kieran C. Murphy, Peter J. Scambler (eds): Velo-cardio-facial syndrome: a model for understanding microdeletion disorders (2005)

    • Ian D. Young

    Book Review 15 November 2005 Pages: 786 - 786