1. Genetics of molybdenum cofactor deficiency

   • J. Reiss

   Review Article Pages: 157 - 163

2. Gene organization and rearrangements at the human Rhesus blood group locus revealed by fiber-FISH analysis

   • Y. Suto
   • Y. Ishikawa
   • T. Juji

   Original Investigation Pages: 164 - 171

3. A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals

   • C. Bombieri
   • S. Giorgi
   • G. Modiano

   Original Investigation Pages: 172 - 178

4. Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation

   • Q. Saleem
   • S. Choudhry
   • S.K. Brahmachari

   Original Investigation Pages: 179 - 187

5. Meiotic segregation analysis of a 14;21 Robertsonian translocation carrier by fluorescence in situ hybridization

   • H. Honda
   • N. Miharu
   • K. Ohama

   Original Investigation Pages: 188 - 193

6. Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients

   • A. Poyau
   • K. Buchet
   • C. Godinot

   Original Investigation Pages: 194 - 205

7. Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA₃)

   • M.I. Rees
   • P. Watts
   • J. Gray

   Original Investigation Pages: 206 - 209

8. Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization

   • L. Voullaire
   • H. Slater
   • L. Wilton

   Original Investigation Pages: 210 - 217

9. A simple and accurate method for determination of microsatellite total allele content differences between DNA pools

   • H.E. Collins
   • H. Li
   • M.F. Seldin

   Original Investigation Pages: 218 - 226

10. SEL1L, the human homolog of C. elegans sel-1: refined physical mapping, gene structure and identification of polymorphic markers

    • I. Biunno
    • L. Bernard
    • M. Zollo

    Original Investigation Pages: 227 - 235

11. Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome

    • B. Parfait
    • D. Chretien
    • P. Rustin

    Original Investigation Pages: 236 - 243

12. Complex inheritance of ABCR mutations in Stargardt disease: linkage disequilibrium, complex alleles, and pseudodominance

    • N.F. Shroyer
    • R.A. Lewis
    • J.R. Lupski

    Original Investigation Pages: 244 - 248

13. Molecular analysis of the genotype-phenotype relationship in factor X deficiency

    • D.S. Millar
    • L. Elliston
    • D.N. Cooper

    Original Investigation Pages: 249 - 257