Contribution of gene conversion in the evolution of the human β-like globin gene family M. N. PapadakisG. P. Patrinos Review article Pages: 117 - 125
World distribution of the T833C/844INS68 CBS in cis double mutation: a reliable anthropological marker G. PepeO. Camacho VanegasR. Abbate Original investigation Pages: 126 - 129
Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibility Sabrina SempriniFrancesca CaponG. Novelli Original investigation Pages: 130 - 134
Supravalvular aortic stenosis: a splice site mutation within the elastin gene results in reduced expression of two aberrantly spliced transcripts Zsolt UrbánVirginia V. MichelsC. D. Boyd Original investigation Pages: 135 - 142
Identification and characterization of mutations in patients with holocarboxylase synthetase deficiency Yoko AokiX. LiKuniaki Narisawa Original investigation Pages: 143 - 148
Estimating European admixture in African Americans by using microsatellites and a microsatellite haplotype (CD4/Alu) G. Destro-BisolRiccardo MavigliaSarah Tishkoff Original investigation Pages: 149 - 157
Further evidence for a synergistic association between APOEɛ4 and BCHE-K in confirmed Alzheimer’s disease H. WiebuschJudes PoirierKeith Schappert Original investigation Pages: 158 - 163
Amplification of Y-chromosomal STRs from ancient skeletal material T. SchultesSusanne HummelBernd Herrmann Original investigation Pages: 164 - 166
Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer B. V. BapatLisa MadlenskySteven Gallinger Original investigation Pages: 167 - 176
Nucleotide sequence diversity in non-coding regions of ALDH2 as revealed by restriction enzyme and SSCP analysis Raymond J. PetersonDavid GoldmanJ. C. Long Original investigation Pages: 177 - 187
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations S. UsamiSatoko AbeWilliam J. Kimberling Original investigation Pages: 188 - 192
1176C Polymorphism in Japanese patients with glycogen storage disease type 1a M. OkuboAsako HorinishiKeisuke Hamada Letter to the editor Pages: 193 - 193
