The neurobeachin gene spans the common fragile site FRA13A Larissa SavelyevaEvgeny SagulenkoManfred Schwab Original Investigation 22 October 2005 Pages: 551 - 558
Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy Sarah A. ShoichetLaurence DuprezVera M. Kalscheuer Original Investigation 25 October 2005 Pages: 559 - 567
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 HsuTianhua NiuXiping Xu Original Investigations 26 October 2005 Pages: 568 - 577
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation Olivier HagensAline DubosAndré Hanauer Original Investigation 26 October 2005 Pages: 578 - 590
Contrasting patterns of Y-chromosome variation in South Siberian populations from Baikal and Altai-Sayan regions Miroslava DerenkoBoris MalyarchukIlia Zakharov Original Investigation 27 October 2005 Pages: 591 - 604
A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3 Muhammad Jawad HassanRegie Lyn P. SantosSuzanne M. Leal Original Investigation 29 October 2005 Pages: 605 - 610
Ring chromosome 15: characterization by array CGH Ian A. GlassKatherine A. RauenPhilip D. Cotter Original Investigation 03 November 2005 Pages: 611 - 617
Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation Liesbet DeprezLieve R. F. ClaesPeter De Jonghe Original Investigation 05 November 2005 Pages: 618 - 625
Admixture-matched case-control study: a practical approach for genetic association studies in admixed populations Hui-Ju TsaiJennifer Y. KhoEsteban González Burchard Original Investigation 05 November 2005 Pages: 626 - 639
A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions K. L. LachlanS. YouingsN. S. Thomas Original Investigation 08 November 2005 Pages: 640 - 651
Population stratification confounds genetic association studies among Latinos Shweta ChoudhryNatasha E. CoyleGenetics of Asthma in Latino Americans (GALA) Study Original Investigation 08 November 2005 Pages: 652 - 664
Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33–q27.3 Peter JohnGhazanfar AliWasim Ahmad Short Report 05 November 2005 Pages: 665 - 667
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 BorgPaweł StankiewiczTadeusz Mazurczak Erratum 23 November 2005 Pages: 668 - 668