1. Diagnosis of human genetic disease using recombinant DNA

   • D. N. Cooper
   • J. Schmidtke

   Review Article Pages: 211 - 236

2. Duplication detection in Japanese Duchenne muscular dystrophy patients and identification of carriers with partial gene deletions using pulsed-field gel electrophoresis

   • Mieko Kodaira
   • Keiko Hiyama
   • Chiyoko Satoh

   Original Investigations Pages: 237 - 243

3. Loss of heterozygosity and K-ras gene mutations in gastric cancer

   • G. N. Ranzani
   • B. Renault
   • D. Amadori

   Original Investigations Pages: 244 - 249

4. Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3–p11.22 region

   • Suzanne M. Cremin
   • Wenda L. Greer
   • Katherine A. Siminovitch

   Original Investigations Pages: 250 - 253

5. Phenylketonuria in Spain: RFLP haplotypes and linked mutations

   • Lourdes R. Desviat
   • Belén Pérez
   • Magdalena Ugarte

   Original Investigations Pages: 254 - 258

6. Human chromosome 11 complements ataxia-telangiectasia cells but does not complement the defect in AT-like Chinese hamster cell mutants

   • W. Jongmans
   • J. Wiegant
   • M. Z. Zdzienicka

   Original Investigations Pages: 259 - 264

7. Retrospective molecular detection of transhyretin Met 111 mutation in a Danish kindred with familial amyloid cardiomyopathy, using DNA from formalin-fixed and paraffin-embedded tissues

   • Bjørn-Yngvar Nordvåg
   • Ida Ranløv
   • M. Raafat El-Gewely

   Original Investigations Pages: 265 - 268

8. Founder effect in a Belgian-Dutch fragile X population

   • Sonja Buyle
   • Edwin Reyniers
   • Patrick J. Willems

   Original Investigations Pages: 269 - 272

9. Genetic and molecular analysis of familial isolated growth hormone deficiency

   • Rosalía Ruiz-Pacheco
   • Pierre Chatelain
   • Charles Sultan

   Original Investigations Pages: 273 - 281

10. Long range restriction map of the von Hippel-Lindau gene region on human chromosome 3p

    • Susanne C. Szymanski
    • Holger Hummerich
    • Elisabeth Schröder

    Original Investigations Pages: 282 - 288

11. Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis

    • Hagit Sereth
    • Tzipora Shoshani
    • Bat-sheva Kerem

    Original Investigations Pages: 289 - 295

12. Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus

    • Agneta Nordenskjöld
    • Fredrik Hedborg
    • Magnus Nordenskjöld

    Short Communications Pages: 296 - 298

13. Genetic mapping of the erythropoietin receptor gene

    • Pertti Sistonen
    • Ann-Liz Träskelin
    • Albert de la Chapelle

    Short Communications Pages: 299 - 301

14. Detection of an exon 53 polymorphism in the dystrophin gene

    • Thomas W. Prior
    • Audrey C. Papp
    • Mary S. Sedra

    Short Communications Pages: 302 - 304

15. Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints

    • R. J. Sinke
    • B. de Leeuw
    • A. Geurts van Kessel

    Short Communications Pages: 305 - 308

16. Fetal cells in the maternal circulation during first trimester in pregnancies

    • Jui-Der Liou
    • Chia C. Pao
    • Shu-Min Kao

    Short Communications Pages: 309 - 311

17. Dinucleotide repeat polymorphisms at the lipoprotein lipase (LPL) locus

    • T. M. Narcisi
    • M. C. Schotz
    • C. C. Shoulders

    OriginalPaper Pages: 312 - 313

18. Announcements

    Announcement Pages: 314 - 314