The Indian Genome Variation database (IGVdb): a project overview The Indian Genome Variation Consortium Review Article 25 August 2005 Pages: 1 - 11
Meprin β metalloprotease gene polymorphisms associated with diabetic nephropathy in the Pima Indians Alexander R. Red EagleRobert L. HansonJudith S. Bond Original Investigation 25 August 2005 Pages: 12 - 22
Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the X-chromosome comprising exon 9 through 51 of the COL4A5 gene Jens Michael HertzUlf PerssonMårten Segelmark Original Investigation 17 August 2005 Pages: 23 - 28
Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder Tomoko MakishimaClara I. RodriguezAndrew J. Griffith Original Investigation 03 August 2005 Pages: 29 - 34
High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas Teresita Díaz de StåhlCaisa M. HanssonJan P. Dumanski Original Investigation 03 August 2005 Pages: 35 - 44
Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardation K. PoirierJ. AbriolT. Bienvenu Original Investigation 03 August 2005 Pages: 45 - 48
Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype–phenotype correlation in Indian patients A. GuptaD. AikathK. Ray Original Investigation 17 August 2005 Pages: 49 - 57
CTLA4 is differentially associated with autoimmune diseases in the Dutch population Alexandra ZhernakovaPeter EerlighBobby P. C. Koeleman Original Investigation 16 July 2005 Pages: 58 - 66
Haplotypes within genes of β-chemokines in 17q11 are associated with multiple sclerosis: a second phase study Tamara VyshkinaBernadette Kalman Original Investigation 03 August 2005 Pages: 67 - 75
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy Tiziano PramparoSalvatore GrossoRoberto Giorda Original Investigation 07 July 2005 Pages: 76 - 81
Dominantly inherited cutaneous small-vessel lymphocytic vasculitis maps to chromosome 6q26–q27 Gabrielle S. SellickRichard J. ColemanRichard S. Houlston Original Investigation 17 August 2005 Pages: 82 - 86
TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort Haiying MengKarl HagerJeffrey R. Gruen Original Investigation 16 August 2005 Pages: 87 - 90
Splicing mutation associated with Rett syndrome and an experimental approach for genetic diagnosis Liron AbuhatziraKirill MakedonskiRuth Shemer Original Investigation 17 August 2005 Pages: 91 - 98
Heightened stress response in primary fibroblasts expressing mutant eIF2B genes from CACH/VWM leukodystrophy patients Liraz KantorHeather P. HardingOrna Elroy-Stein Original Investigation 23 July 2005 Pages: 99 - 106
Insights into the mutational history and prevalence of SCA1 in the Indian population through anchored polymorphisms Uma MittalSangeeta SharmaMitali Mukerji Original Investigation 17 August 2005 Pages: 107 - 114
Maternal lineages and Alzheimer disease risk in the Old Order Amish Joelle M. van der WaltWilliam K. ScottMargaret A. Pericak-Vance Original Investigation 03 August 2005 Pages: 115 - 122
Meta-analysis of the association of CTLA-4 exon-1 +49A/G polymorphism with rheumatoid arthritis Shizhong HanYao LiYi Xie Original Investigation 17 August 2005 Pages: 123 - 132
A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3 Pedro FernandezJohanna Moolman-SmookValerie Corfield Original Investigation 06 August 2005 Pages: 133 - 137
Susceptibility to typhoid fever is associated with a polymorphism in the cystic fibrosis transmembrane conductance regulator (CFTR) Esther van de VosseSoegianto AliJaap T. van Dissel Short Report 03 August 2005 Pages: 138 - 140
William Bateson, human genetics and medicine Peter S. Harper Historical & Personal Perspectives 17 August 2005 Pages: 141 - 151
