Mutational analysis of the human FATE gene in 144 infertile men Christian OlesenJoachim SilberNiels Tommerup Original Investigation 14 June 2003 Pages: 195 - 201
Analysis of zinc transporter, hZnT4 (Slc30A4), gene expression in a mammary gland disorder leading to reduced zinc secretion into milk Agnes MichalczykGeorge VarigosM. Leigh Ackland Original Investigation 13 May 2003 Pages: 202 - 210
Markers informative for ancestry demonstrate consistent megabase-length linkage disequilibrium in the African American population Heather E. Collins-SchrammBill ChimaMichael F. Seldin Original Investigation 03 June 2003 Pages: 211 - 219
Increased variation in mtDNA in patients with familial sensorineural hearing impairment Mervi S. LehtonenJukka S. MoilanenKari Majamaa Original Investigation 12 June 2003 Pages: 220 - 227
Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect Kristin AstromJoel E. CohenBora E. Baysal Original Investigation 17 June 2003 Pages: 228 - 237
Lung cancer risk in germline p53 mutation carriers: association between an inherited cancer predisposition, cigarette smoking, and cancer risk Shih-Jen HwangLi Shu-Chung ChengLouise C. Strong Original Investigation 11 June 2003 Pages: 238 - 243
The origins and genetic structure of three co-resident Chinese Muslim populations: the Salar, Bo'an and Dongxiang Wei WangCheryl WiseAlan H. Bittles Original Investigation 21 May 2003 Pages: 244 - 252
Comparison of strategies for selecting single nucleotide polymorphisms for case/control association studies Qiqing HuangYun-xin FuEric Boerwinkle Original Investigation 17 June 2003 Pages: 253 - 257
Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease Denise HaroldTimothy PeirceLesley Jones Original Investigation 21 May 2003 Pages: 258 - 267
Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon José A. J. M. van den HurkDorien J. R. van de PolFrans P. M. Cremers Original Investigation 25 June 2003 Pages: 268 - 275
The association between Japanese primary open-angle glaucoma and normal tension glaucoma patients and the optineurin gene Sa TangYoshiki TodaZentaro Yamagata Original Investigation 17 June 2003 Pages: 276 - 279
Impact of public health strategies on the birth prevalence of cystic fibrosis in Brittany, France Virginie ScotetMarie-Pierre AudrézetClaude Férec Original Investigation 27 May 2003 Pages: 280 - 285
Increased prevalence of CFTR mutations and variants and decreased chloride secretion in primary sclerosing cholangitis Sunil ShethJulie C. SheaSteven D. Freedman Original Investigation 03 June 2003 Pages: 286 - 292
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13 Lisbeth TranebjaergTanya M. TeslovichDietrich A. Stephan Short Report 17 June 2003 Pages: 293 - 295