1. Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities

   • E. Schröck
   • T. Veldman
   • Thomas Ried

   Original investigation Pages: 255 - 262

2. Refined genetic localization of the Best disease gene in 11q13 and physical mapping of linked markers on radiation hybrids

   • Caroline Graff
   • Anna Eriksson
   • Claes Wadelius

   Original investigation Pages: 263 - 270

3. Phenotype-genotype correlation in haemochromatosis subjects

   • C. Mura
   • Jean-Baptiste Nousbaum
   • Claude Ferec

   Original investigation Pages: 271 - 276

4. Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25

   • Joan E. Pellegrino
   • Roberta A. V. George
   • P. F. Chance

   Original investigation Pages: 277 - 283

5. The human histone gene cluster at the D6S105 locus

   • Werner Albig
   • D. Doenecke

   Original investigation Pages: 284 - 294

6. Clonal chromosome aberrations are present in vivo in synovia and osteophytes from patients with osteoarthritis

   • K. Broberg
   • Janusz Limon
   • Fredrik Mertens

   Original investigation Pages: 295 - 298

7. Spontaneous and induced aneuploidy in peripheral blood lymphocytes of patients with Alzheimer’s disease

   • L. Migliore
   • Anna Testa
   • Ubaldo Bonuccelli

   Original investigation Pages: 299 - 305

8. TRP64ARG β3-adrenergic receptor and obesity in Mexican Americans

   • K. Silver
   • Braxton D. Mitchell
   • A. R. Shuldiner

   Original investigation Pages: 306 - 311

9. Detection of heterozygous carriers of the ataxia-telangiectasia (ATM) gene by G₂ phase chromosomal radiosensitivity of peripheral blood lymphocytes

   • A. Tchirkov
   • Jacques-Olivier Bay
   • Pierre Verrelle

   Original investigation Pages: 312 - 316

10. Mapping the multiple self-healing squamous epithelioma (MSSE) gene and investigation of xeroderma pigmentosum group A (XPA) and PATCHED (PTCH) as candidate genes

    • F. M. Richards
    • David R. Goudie
    • M. A. Ferguson-Smith

    Original investigation Pages: 317 - 322

11. Factor VIII gene mutations found by a comparative study of SSCP, DGGE and CMC and their analysis on a molecular model of factor VIII protein

    • R. Schwaab
    • J. Oldenburg
    • K. Michaelides

    Original investigation Pages: 323 - 332

12. Dihydropyrimidine dehydrogenase (DPD) deficiency: identification and expression of missense mutations C29R, R886H and R235W

    • P. Vreken
    • A. B. P. Van Kuilenburg
    • A. H. van Gennip

    Original investigation Pages: 333 - 338

13. Double trisomy in spontaneous abortions

    • K. S. Reddy

    Original investigation Pages: 339 - 345

14. Alu-splice PCR: a simple method to isolate exon-containing fragments from cloned human genomic DNA

    • Juan-José Fuentes
    • Carles Pucharcós
    • X. Estivill

    Original investigation Pages: 346 - 350

15. A rapid screening method for hepatocyte nuclear factor 1 alpha frameshift mutations; prevalence in maturity-onset diabetes of the young and late-onset non-insulin dependent diabetes

    • Timothy M. Frayling
    • Michael P. Bulman
    • Sian Ellard

    Original investigation Pages: 351 - 354

16. Incidence of the mucopolysaccharidoses in Northern Ireland

    • J. Nelson

    Original investigation Pages: 355 - 358

17. Inherited susceptibility to several cancers but absence of linkage between dysplastic nevus syndrome and CDKN2A in a melanoma family with a mutation in the CDKN2A (P16INK4A) gene

    • S. Puig
    • Anna Ruiz
    • Xavier Estivill

    Original investigation Pages: 359 - 364

18. High heterogeneity for cystic fibrosis in Spanish families: 75 mutations account for 90% of chromosomes

    • Teresa Casals
    • Maria D. Ramos
    • X. Estivill

    Original investigation Pages: 365 - 370

19. Alternative splicing in PAX2 generates a new reading frame and an extended conserved coding region at the carboxy terminus

    • Kamiab Tavassoli
    • Wolfgang Rüger
    • Jürgen Horst

    Original investigation Pages: 371 - 375

20. Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14–q21 by homozygosity mapping

    • Martin Walter Laass
    • Hans Christian Hennies
    • André Reis

    Original investigation Pages: 376 - 382