Gene organization and rearrangements at the human Rhesus blood group locus revealed by fiber-FISH analysis Y. SutoY. IshikawaT. Juji Original Investigation Pages: 164 - 171
A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals C. BombieriS. GiorgiG. Modiano Original Investigation Pages: 172 - 178
Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation Q. SaleemS. ChoudhryS.K. Brahmachari Original Investigation Pages: 179 - 187
Meiotic segregation analysis of a 14;21 Robertsonian translocation carrier by fluorescence in situ hybridization H. HondaN. MiharuK. Ohama Original Investigation Pages: 188 - 193
Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients A. PoyauK. BuchetC. Godinot Original Investigation Pages: 194 - 205
Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3) M.I. ReesP. WattsJ. Gray Original Investigation Pages: 206 - 209
Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization L. VoullaireH. SlaterL. Wilton Original Investigation Pages: 210 - 217
A simple and accurate method for determination of microsatellite total allele content differences between DNA pools H.E. CollinsH. LiM.F. Seldin Original Investigation Pages: 218 - 226
SEL1L, the human homolog of C. elegans sel-1: refined physical mapping, gene structure and identification of polymorphic markers I. BiunnoL. BernardM. Zollo Original Investigation Pages: 227 - 235
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome B. ParfaitD. ChretienP. Rustin Original Investigation Pages: 236 - 243
Complex inheritance of ABCR mutations in Stargardt disease: linkage disequilibrium, complex alleles, and pseudodominance N.F. ShroyerR.A. LewisJ.R. Lupski Original Investigation Pages: 244 - 248
Molecular analysis of the genotype-phenotype relationship in factor X deficiency D.S. MillarL. EllistonD.N. Cooper Original Investigation Pages: 249 - 257
