Advances in osteoclast biology resulting from the study of osteopetrotic mutations T. Segovia-SilvestreA. V. Neutzsky-WulffK. Henriksen Review Article 06 November 2008 Pages: 561 - 577
Lactose digestion and the evolutionary genetics of lactase persistence Catherine J. E. IngramCharlotte A. MulcareDallas M. Swallow Review Article 26 November 2008 Pages: 579 - 591
Genomewide association study for susceptibility genes contributing to familial Parkinson disease Nathan PankratzJemma B. WilkThe PSG—PROGENI and GenePD Investigators, Coordinators and Molecular Genetic Laboratories Original Investigations 06 November 2008 Pages: 593 - 605
A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia Javier CostasNoa CarreraÁngel Carracedo Original Investigation 06 November 2008 Pages: 607 - 613
A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype Abidemi A. AdegbolaMichael L. GonzalesGerald F. Cox Original Investigation 07 November 2008 Pages: 615 - 623
Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas F. C. ConnellP. OstergaardLymphoedema Consortium Original Investigation 12 November 2008 Pages: 625 - 631
Increased constraints on MC4R during primate and human evolution David A. HughesAnke HinneyMark Stoneking Original Investigation Open access 15 November 2008 Pages: 633 - 647
Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation Hussein DaoudNicolas GruchySylvain Briault Original Investigation 16 November 2008 Pages: 649 - 658
The joint association between F5 gene polymorphisms and maternal smoking during pregnancy on preterm delivery Yunxian YuHui-Ju TsaiXiaobin Wang Original Investigation 20 November 2008 Pages: 659 - 668
A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2–q12.3 Arunima ChatterjeeRajeev JalviAnuranjan Anand Original Investigation 22 November 2008 Pages: 669 - 675