1. Analysis of a paracentric inversion in human oocytes: nonhomologous pairing in pachytene

   • E.Y. Cheng
   • Y.J. Chen
   • S.M. Gartler

   Original Investigation Pages: 191 - 196

2. Genetic contribution of the BAT2 gene microsatellite polymorphism to the age-at-onset of insulin-dependent diabetes mellitus

   • M. Hashimoto
   • N. Nakamura
   • M. Nishimura

   Original Investigation Pages: 197 - 199

3. Novel and recurrent mutations in the tyrosinase gene and the P gene in the German albino population

   • L. Passmore
   • B. Kaesmann-Kellner
   • B. Weber

   Original Investigation Pages: 200 - 210

4. Alpha-tectorin involvement in hearing disabilities: one gene – two phenotypes

   • J. Balciuniene
   • N. Dahl
   • E.E. Jazin

   Original Investigation Pages: 211 - 216

5. Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation

   • J. Del-Favero
   • D. Goossens
   • C. Van Broeckhoven

   Original Investigation Pages: 217 - 225

6. Dopa-responsive dystonia induced by a recessive GTP cyclohydrolase I mutation

   • W.-L. Hwu
   • P.-J. Wang
   • Y.-M. Lee

   Original Investigation Pages: 226 - 230

7. DGGE screening of PKD1 gene reveals novel mutations in a large cohort of 146 unrelated patients

   • R.A. Perrichot
   • B. Mercier
   • C. Ferec

   Original Investigation Pages: 231 - 239

8. A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity

   • B. Burwinkel
   • S.A. Sanjad
   • M.W. Kilimann

   Original Investigation Pages: 240 - 243

9. Molecular genetics of human prion diseases in Germany

   • O. Windl
   • A. Giese
   • H.A. Kretzschmar

   Original Investigation Pages: 244 - 252

10. Linkage of interleukin 6 locus to human osteopenia by sibling pair analysis

    • N. Ota
    • S.C. Hunt
    • M. Emi

    Original Investigation Pages: 253 - 257

11. Rapid FMR1-protein analysis of fetal blood: an enhancement of prenatal diagnostics

    • N. Lambiris
    • H. Peters
    • R. Willemsen

    Original Investigation Pages: 258 - 260

12. Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

    • K.L. Friend
    • D. Crimmins
    • R.I. Richards

    Original Investigation Pages: 261 - 265

13. Relationship between clinical phenotype, semen parameters and aneuploidy frequency in sperm nuclei of 50 infertile males

    • Nathalie Rives
    • Alexia Saint Clair
    • Bertrand Macé

    Original Investigation Pages: 266 - 272

14. Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome

    • C.A. Joyce
    • A. Sharp
    • I.K. Temple

    Original Investigation Pages: 273 - 280

15. Vitamin D receptor polymorphisms as markers in prostate cancer

    • L. Correa-Cerro
    • P. Berthon
    • W. Vogel

    Original Investigation Pages: 281 - 287

16. Reorganization of the sex-determining pathway with the evolution of placentation

    • U. Wolf

    Food For Thought Pages: 288 - 292