An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants Charles E. OgburnJunko OshimaG. M. Martin Original investigation Pages: 121 - 125
Association of transferrin C2 allele with late-onset Alzheimer’s disease Kazuhiko NamekataMasaki ImagawaY. Ihara Original investigation Pages: 126 - 129
Fine mapping of the gene for autosomal dominant juvenile-onset glaucoma with iridogoniodysgenesis in 6p25-tel C. GraffTord JerndalClaes Wadelius Original investigation Pages: 130 - 134
Evolutionary origins of two tightly linked mutations in arylsulfatase-A pseudodeficiency Rebecca OttJohn S. WayeP. Chang Original investigation Pages: 135 - 140
Evidence for convergent evolution of A and B blood group antigens in primates C. O’hUiginAkie SatoJan Klein Original investigation Pages: 141 - 148
A novel source of highly specific chromosome painting probes for human karyotype analysis derived from primate homologues Stefan MüllerPatricia C. M. O’BrienJ. Wienberg Original investigation Pages: 149 - 153
Gene structure and allelic expression assay of the human GLI3 gene S. KangMarjorie RosenbergL. G. Biesecker Original investigation Pages: 154 - 157
ACP1 and human adaptability 2. Association with season of conception Fulvia Gloria-BottiniNazzareno LucariniE. Bottini Original investigation Pages: 158 - 164
A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix H. WinterMichael A. RogersJürgen Schweizer Original investigation Pages: 165 - 169
Phosphorylase-kinase-deficient liver glycogenosis with an unusual biochemical phenotype in blood cells associated with a missense mutation in the β subunit gene (PHKB) Barbara BurwinkelShimon W. MosesM. W. Kilimann Original investigation Pages: 170 - 174
Inv(10)(p11.2q21.2), a variant chromosome M. N. CollinsonAndrew M. FisherPaul Roberts Original investigation Pages: 175 - 180
RB1 deletion in gonadoblastoma in an XY female Sylvie AntoniniAngela S. BarbosaA. M. Vianna-Morgante Original investigation Pages: 181 - 185
No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome Rachel PessoG. BarkaiE. Friedman Original investigation Pages: 186 - 189
Identification of an amplified gene cluster in glioma including two novel amplified genes isolated by exon trapping Hans-Werner MuellerArmin MichelE. Meese Original investigation Pages: 190 - 197
The human lysyl oxidase-like gene maps between STS markers D15S215 and GHLC.GCT7C09 on chromosome 15 Zoltán SzabóElizabeth LightK. Csiszár Original investigation Pages: 198 - 200
Pepsinogen polymorphism in the Indian population and its association with duodenal ulcer A. VenkateshwariA. VidyasagarN. Pratibha Original investigation Pages: 201 - 204
Assignment of human plasma methylumbelliferyl-tetra-N-acetylchitotetraoside hydrolase or chitinase to chromosome 1q by a linkage study H. EibergWilfried Richard Den Tandt Original investigation Pages: 205 - 207
Genotype-phenotype correlation in cystic fibrosis patients compound heterozygous for the A455E mutation M. De BraekeleerChristian AllardGervais Aubin Original investigation Pages: 208 - 211
Genetic linkage study of a major susceptibility locus (D2S125) in a British population of non-insulin dependent diabetic sib-pairs using a simple non-isotopic screening method Andrew W. ThomasEmma J. SherrattJohn C. Alcolado Original investigation Pages: 212 - 213
Sequence analysis of long FMR1 arrays in the Japanese population: insights into the generation of long (CGG) n tracts M. C. HirstTadao ArinamiCharles D. Laird Original investigation Pages: 214 - 218
Asynchronous replication of p53 and 21q22 loci in chronic lymphocytic leukemia A. AmielTali LitmanovichMoshe D. Fejgin Original investigation Pages: 219 - 222
Dual blastomere analysis improves reliability of preimplantation trembler mouse diagnosis H. SagoH.-S. KimRoger V. Lebo Original investigation Pages: 223 - 228
Novel stop and frameshifting mutations in the autosomal dominant polycystic kidney disease 2 (PKD2) gene Miguel ViribayTomohito HayashiJosé L. San Millán Original investigation Pages: 229 - 234
Exclusion of PPEF as the gene causing X-linked juvenile retinoschisis E. van de VosseBrunella FrancoArthur A. B. Bergen Original investigation Pages: 235 - 237
Familial Mediterranian fever: clastogenic plasma factors correlated with increased O2 –– production by neutrophils T. SarkisianI. EmeritP. Filipe Original investigation Pages: 238 - 242
Serotonin transporter protein (SLC6A4) allele and haplotype frequencies and linkage disequilibria in African- and European-American and Japanese populations and in alcohol-dependent subjects J. GelernterHenry KranzlerJoseph F. Cubells Rapid communication Pages: 243 - 246
No mitochondrial cytochrome oxidase (COX) gene mutations in 18 cases of COX deficiency Béatrice ParfaitAgnès PercheronAgnès Rötig Rapid communication Pages: 247 - 250