1. Allelic polymorphisms and RFLP in the human immunoglobulin lambda light chain locus

   • Marie-Paule Lefranc
   • Nathalie Pallarès
   • Jean-Pol Frippiat

   Review article Pages: 361 - 369

2. Combined RxFISH/G-banding allows refined karyotyping of solid tumors

   • Francesca Micci
   • Manuel R. Teixeira
   • Sverre Heim

   Original investigation Pages: 370 - 375

3. A high degree of aneuploidy in frozen-thawed human preimplantation embryos

   • E. Iwarsson
   • Monalill Lundqvist
   • Elisabeth Blennow

   Original investigation Pages: 376 - 382

4. The mutation spectrum of the bestrophin protein – functional implications

   • B. Bakall
   • Towa Marknell
   • Claes Wadelius

   Original investigation Pages: 383 - 389

5. Phenylketonuria mutations in Germany

   • J. Zschocke
   • Georg F. Hoffmann

   Original investigation Pages: 390 - 398

6. Enrichment of fetal trophoblasts and nucleated erythrocytes from maternal blood by an immunomagnetic colloid system

   • Tse Hui Lim
   • Ann Tan
   • Victor Hng Hang Goh

   Original investigation Pages: 399 - 404

7. Estimates of sperm sex chromosome disomy and diploidy rates in a 47,XXY/46,XY mosaic Klinefelter patient

   • Alvin Soon Tiong Lim
   • Yang Fong
   • Su Ling Yu

   Original Investigation Pages: 405 - 409

8. Exclusion of RAI2 as the causative gene for Nance-Horan syndrome

   • Susannah M. Walpole
   • Nathalie Ronce
   • Annick Toutain

   Original investigation Pages: 410 - 411

9. Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)

   • Anna M. Estop
   • Kathy M. Cieply
   • Eleanor Feingold

   Original investigation Pages: 412 - 417

10. A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene

    • Carl E. G. Bruder
    • Koichi Ichimura
    • J. P. Dumanski

    Original investigation Pages: 418 - 424

11. Analysis of the mutational spectrum of the FGFR2 gene in Pfeiffer syndrome

    • Laura R. Cornejo-Roldan
    • Erich Roessler
    • M. Muenke

    Original investigation Pages: 425 - 431

12. Association between coding variability in the LRP gene and the risk of late-onset Alzheimer’s disease

    • Fabienne Wavrant-DeVrièze
    • Jean-Charles Lambert
    • Fred Van Leuven

    Short Report Pages: 432 - 434

13. A deletion/insertion leading to the generation of a direct repeat as a result of slipped mispairing and intragenic recombination in the factor VIII gene

    • Kamiab Tavassoli
    • Antonin Eigel
    • Jürgen Horst

    Food for thought Pages: 435 - 437

14. Neurofibromatosis type 1 from genotype to phenotype: M. Upadhyaya and D. N. Cooper BIOS Scientific Publishers (230 pages), ISBN 1-859-961 91-6, £67.50, Hardback

    • Richard Hughes

    Book review Pages: 438 - 438

15. Genetics and tuberculosis. Novartis Foundation Symposium 217: D. J. Chadwick, G. Cardew (Editors) John Wiley and Sons (269 pages), ISBN 0-471-98261-X, £ 57.50, Hardcover

    • Melanie Newport

    Book review Pages: 439 - 440

16. Gene Symbol: AGXT Disease: Primary Hyperoxaluria type I

    • A. Amoroso
    • D. Pirulli
    • F. Florian

    Human gene mutations Pages: 441 - 441