1. Scandinavian CDG-Ia patients: genotype/phenotype correlation and geographic origin of founder mutations

   • Anna Erlandson
   • Cecilia Bjursell
   • Tommy Martinsson

   Original Investigation Pages: 359 - 367

2. Delineation of the critical interval for the familial exudative vitreoretinopathy gene by linkage and haplotype analysis

   • Hiroyuki Kondo
   • Ken Ohno
   • Kenshi Hayashi

   Original Investigation Pages: 368 - 375

3. DHPLC-based germline mutation screening in the analysis of the VHL tumor suppressor gene: usefulness and limitations

   • Bettina Klein
   • Gregor Weirich
   • Hiltrud Brauch

   Original Investigation Pages: 376 - 384

4. Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians

   • Mustafa Tekin
   • Nejat Akar
   • Arti Pandya

   Original Investigation Pages: 385 - 389

5. Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA)

   • J. Meuleman
   • G. Kuhlenbäumer
   • V. Timmerman

   Original Investigation Pages: 390 - 393

6. Refinement of the chromosome 5p locus for craniometaphyseal dysplasia

   • D. Chandler
   • S. Tinschert
   • P. Nürnberg

   Original Investigation Pages: 394 - 397

7. Oto-facio-cervical (OFC) syndrome is a contiguous gene deletion syndrome involving EYA1: molecular analysis confirms allelism with BOR syndrome and further narrows the Duane syndrome critical region to 1 cM

   • Sarah Rickard
   • Michael Parker
   • Maria Bitner-Glindzicz

   Original Investigation Pages: 398 - 403

8. Molecular and functional characterisation of mild MCAD deficiency

   • Johannes Zschocke
   • Andreas Schulze
   • Ertan Mayatepek

   Original Investigation Pages: 404 - 408

9. Cloning and characterization of the human GFRA2 locus and investigation of the gene in Hirschsprung disease

   • Judith B. Vanhorne
   • Oliver Gimm
   • Lois M. Mulligan

   Original Investigation Pages: 409 - 415

10. Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutations

    • E. Serra
    • E. Ars
    • C. Lázaro

    Original Investigation Pages: 416 - 429

11. Evidence for a prostate cancer linkage to chromosome 20 in 159 hereditary prostate cancer families

    • Siqun L. Zheng
    • Jianfeng Xu
    • William B. Isaacs

    Original Investigation Pages: 430 - 435

12. Topoisomerase-I- and Alu-mediated genomic deletions of the APC gene in familial adenomatous polyposis

    • Xia Cao
    • Kong Eu
    • Peh Cheah

    Short Report Pages: 436 - 442