Current status of the E23K Kir6.2 polymorphism: implications for type-2 diabetes Michael J. RiedelDiana C. SteckleyPeter E. Light Review Article 23 November 2004 Pages: 133 - 145
Association of α2-HS glycoprotein (AHSG, fetuin-A) polymorphism with AHSG and phosphate serum levels Motoki OsawaWei TianKazuo Umetsu Original Investigation 09 December 2004 Pages: 146 - 151
Ocular refraction: heritability and genome-wide search for eye morphometry traits in an isolated Sardinian population Ginevra BiinoMaria Antonietta PalmasMario Pirastu Original Investigation 21 December 2004 Pages: 152 - 159
Expression studies of mutations underlying Taiwanese Hunter syndrome (mucopolysaccharidosis type II) Jui-Hung ChangShuan-Pei LinGuey-Jen Lee-Chen Original Investigation 22 December 2004 Pages: 160 - 166
An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22 Thomas G. SabaAlexandre MontpetitChristian A. Drouin Original Investigation 25 November 2004 Pages: 167 - 171
Variation in meiotic recombination frequencies among human males Fei SunKiril TrpkovRenée H. Martin Original Investigation 01 December 2004 Pages: 172 - 178
Confirmation of the HPCX prostate cancer predisposition locus in large Utah prostate cancer pedigrees James M. FarnhamNicola J. CampLisa A. Cannon Albright Original Investigation 08 December 2004 Pages: 179 - 185
Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II Jung-Wook KimJan C-C HuJames P. Simmer Original Investigation 08 December 2004 Pages: 186 - 191
Ala45Thr polymorphism of the NEUROD1 gene and diabetes susceptibility: a meta-analysis Fotini K. KavvouraJohn P. A. Ioannidis Original Investigation 11 December 2004 Pages: 192 - 199
The (GT) n polymorphism and haplotype of the COL1A2 gene, but not the (AAAG) n polymorphism of the PTHR1 gene, are associated with bone mineral density in Chinese Shu-Feng LeiFei-Yan DengHong-Wen Deng Original Investigation 14 December 2004 Pages: 200 - 207
Oligogenic combinations associated with breast cancer risk in women under 53 years of age Christopher E. AstonDavid A. RalphEldon R. Jupe Original Investigation 21 December 2004 Pages: 208 - 221
Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L Bei-sha TangGuo-hua ZhaoHe-ping Dai Short Report 23 November 2004 Pages: 222 - 224
The USH1C 216G→A splice-site mutation results in a 35-base-pair deletion Jennifer LentzSevtap SavasBronya Keats Short Report 01 December 2004 Pages: 225 - 227
Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader–Willi syndrome Maren RunteRaymonda VaronKarin Buiting Short Report 23 November 2004 Pages: 228 - 230