Allelic polymorphisms and RFLP in the human immunoglobulin lambda light chain locus Marie-Paule LefrancNathalie PallarèsJean-Pol Frippiat Review article Pages: 361 - 369
Combined RxFISH/G-banding allows refined karyotyping of solid tumors Francesca MicciManuel R. TeixeiraSverre Heim Original investigation Pages: 370 - 375
A high degree of aneuploidy in frozen-thawed human preimplantation embryos E. IwarssonMonalill LundqvistElisabeth Blennow Original investigation Pages: 376 - 382
The mutation spectrum of the bestrophin protein – functional implications B. BakallTowa MarknellClaes Wadelius Original investigation Pages: 383 - 389
Phenylketonuria mutations in Germany J. ZschockeGeorg F. Hoffmann Original investigation Pages: 390 - 398
Enrichment of fetal trophoblasts and nucleated erythrocytes from maternal blood by an immunomagnetic colloid system Tse Hui LimAnn TanVictor Hng Hang Goh Original investigation Pages: 399 - 404
Estimates of sperm sex chromosome disomy and diploidy rates in a 47,XXY/46,XY mosaic Klinefelter patient Alvin Soon Tiong LimYang FongSu Ling Yu Original Investigation Pages: 405 - 409
Exclusion of RAI2 as the causative gene for Nance-Horan syndrome Susannah M. WalpoleNathalie RonceAnnick Toutain Original investigation Pages: 410 - 411
Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11) Anna M. EstopKathy M. CieplyEleanor Feingold Original investigation Pages: 412 - 417
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. BruderKoichi IchimuraJ. P. Dumanski Original investigation Pages: 418 - 424
Analysis of the mutational spectrum of the FGFR2 gene in Pfeiffer syndrome Laura R. Cornejo-RoldanErich RoesslerM. Muenke Original investigation Pages: 425 - 431
Association between coding variability in the LRP gene and the risk of late-onset Alzheimer’s disease Fabienne Wavrant-DeVrièzeJean-Charles LambertFred Van Leuven Short Report Pages: 432 - 434
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 TavassoliAntonin EigelJürgen Horst Food for thought Pages: 435 - 437
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
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
Gene Symbol: AGXT Disease: Primary Hyperoxaluria type I A. AmorosoD. PirulliF. Florian Human gene mutations Pages: 441 - 441
