Finnish Disease Heritage II: population prehistory and genetic roots of Finns Reijo Norio Review Article 08 March 2003 Pages: 457 - 469
The Finnish disease heritage III: the individual diseases Reijo Norio Review Article 08 March 2003 Pages: 470 - 526
Genome-wide targeted search for human specific and polymorphic L1 integrations Anton BuzdinSvetlana UstyugovaEugene Sverdlov Original Investigation 25 February 2003 Pages: 527 - 533
Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica Luis G. Carvajal-CarmonaRoel OphoffAndrés Ruiz-Linares Original Investigation 25 February 2003 Pages: 534 - 541
Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics Clare L. ScottMark A. JenkinsJohn L. Hopper Original Investigation 25 February 2003 Pages: 542 - 551
Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol Ching Yin LeeLarbi KrimbouMichel Marcil Original Investigation 27 February 2003 Pages: 552 - 562
Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt −1) in the NDUFS4 gene in Leigh syndrome Paule BénitJulie SteffannAgnès Rötig Original Investigation 04 March 2003 Pages: 563 - 566
Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p Dennis DraynaHilary CoonMark Leppert Original Investigation 06 March 2003 Pages: 567 - 572
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse H. PeetersP. DebeerK. Devriendt Original Investigation 27 February 2003 Pages: 573 - 580
Prediction of clinical outcome with microarray data: a partial least squares discriminant analysis (PLS-DA) approach Miguel Pérez-EncisoMichel Tenenhaus Original Investigation 27 February 2003 Pages: 581 - 592
Genetic linkage of Francois-Neetens fleck (mouchetée) corneal dystrophy to chromosome 2q35 Xiaodong JiaoFrancis L. MunierJ. Fielding Hejtmancik Original Investigation 27 February 2003 Pages: 593 - 599
A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle Glaucoma Barbara NemesureXiaodong JiaoBarbados Family Study Group Original Investigation 04 March 2003 Pages: 600 - 609
Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels Coleen M. DamcottEleanor FeingoldRobert E. Ferrell Original Investigation 13 March 2003 Pages: 610 - 616
No evidence of fetal DNA persistence in maternal plasma after pregnancy Maddalena SmidSilvia GalbiatiLaura Cremonesi Short Report 27 February 2003 Pages: 617 - 618
Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia James MacphersonAndrew WaghornPatricia Jacobs Letter to the Editors 27 February 2003 Pages: 619 - 620
G. Evers-Kiebooms, M.W. Zoeteweij, P.S. Harper (eds): Prenatal testing for late onset neurogenetic diseases Aad Tibben Book Review 04 March 2003 Pages: 621 - 622
European Academy of Andrology (EAA) International Symposium Announcements 11 April 2003 Pages: 623 - 623