Publication of microarray results Ulrich MüllerManuel B. GraeberJames R. Lupski Editorial 26 April 2003 Pages: 155 - 155
Dementia with Lewy bodies: disease concept and genetics Manuel B. GraeberUlrich Müller Review Article 26 July 2003 Pages: 157 - 162
Gene expression profiling of Duchenne muscular dystrophy skeletal muscle Judith N. HaslettDespina SanoudouLouis M. Kunkel Original Article 16 April 2003 Pages: 163 - 171
Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus Désirée von TellCarl E. G. BruderGabrielle Åhlberg Original Article 27 June 2003 Pages: 173 - 177
Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the region Danqing ZhuMarina KennersonGarth Nicholson Original Article 22 May 2003 Pages: 179 - 183
Haplotype analysis of the ETM2 locus in familial essential tremor Joseph J. HigginsJoseph JankovicMelanie U. Ruszczyk Original Article 22 May 2003 Pages: 185 - 189
Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family Alejandro LealCorinna BerghoffDieter Heuss Original Article 05 July 2003 Pages: 191 - 197
A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystonia David K. SimonJennifer FriedmanMark A. Tarnopolsky Original Article 17 May 2003 Pages: 199 - 205
Association of dopamine D4 receptor (DRD4) exon III repeat polymorphism with temperament in 3-year-old infants Alessandro De LucaMario RizzardiBruno Dallapiccola Original Article 27 March 2003 Pages: 207 - 212
Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2 U. FinckhK. van HadelnA. Gal Original Article 24 July 2003 Pages: 213 - 217
Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson′s disease Alexander ZimprichFriedrich AsmusThomas Gasser Letter to the Editors 25 June 2003 Pages: 219 - 220
Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis Ammar Al-ChalabiValerie K. HansenRobert H. Brown Jr Letter to the Editor 27 May 2003 Pages: 221 - 222