Clinical and molecular studies in 15 females with ring X chromosomes: implications for r(X) formation and mental development Mari MatsuoKoji MuroyaTsutomu Ogata Original Investigation Pages: 433 - 439
Characterization of the human nebulette gene: a polymorphism in an actin-binding motif is associated with nonfamilial idiopathic dilated cardiomyopathy Takuro ArimuraTakeyuki NakamuraAkinori Kimura Original Investigation Pages: 440 - 451
Differential somatic CAG repeat instability in variable brain cell lineage in dentatorubral pallidoluysian atrophy (DRPLA): a laser-captured microdissection (LCM)-based analysis Hidetaka WatanabeFumiaki TanakaGen Sobue Original Investigation Pages: 452 - 457
Identification of an intronic regulatory element in the human protein C (PROC) gene Monee ShamsherNadia ChuzhanovaLutz-Peter Berg Original Investigation Pages: 458 - 465
Complex adaptive systems and human health: the influence of common genotypes of the apolipoprotein E (ApoE) gene polymorphism and age on the relational order within a field of lipid metabolism traits Kim ZerbaRobert FerrellCharles Sing Original Investigation Pages: 466 - 475
Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome? Melisa BaptistaUna FairbrotherAnna Kessling Original Investigation Pages: 476 - 482
High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC) Johanna WolfordDalia BluntMichal Prochazka Original Investigation Pages: 483 - 487
Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools Bastiaan HoogendoornNadine NortonMichael O'Donovan Original Investigation Pages: 488 - 493
Real-time quantitative polymerase chain reaction Nina AarskogChristian Vedeler Original Investigation Pages: 494 - 498
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen Jessica TysonLisbeth TranebjærgMaria Bitner-Glindzicz Original Investigation Pages: 499 - 503
Evolutionary history of the mtDNA 9-bp deletion in Chinese populations and its relevance to the peopling of east and southeast Asia Yong-Gang YaoW. WatkinsYa-Ping Zhang Original Investigation Pages: 504 - 512
Association analysis of GABAA β2 and γ2 gene polymorphisms with event-related prefrontal activity in man Georg WintererMichael SmolkaThomas Sander Original Investigation Pages: 513 - 518
Refined localization of a gene for pediatric gastroesophageal reflux makes HTR2A an unlikely candidate gene Fen HuJ. PostRobert Preston Original Investigation Pages: 519 - 525
Human variant glucose-6-phosphate transporter is active in microsomal transport Baochuan LinChi-Jiunn PanJanice Chou Short Report Pages: 526 - 529