Diagnosis of human genetic disease using recombinant DNA D. N. CooperJ. Schmidtke Review Article Pages: 211 - 236
Duplication detection in Japanese Duchenne muscular dystrophy patients and identification of carriers with partial gene deletions using pulsed-field gel electrophoresis Mieko KodairaKeiko HiyamaChiyoko Satoh Original Investigations Pages: 237 - 243
Loss of heterozygosity and K-ras gene mutations in gastric cancer G. N. RanzaniB. RenaultD. Amadori Original Investigations Pages: 244 - 249
Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3–p11.22 region Suzanne M. CreminWenda L. GreerKatherine A. Siminovitch Original Investigations Pages: 250 - 253
Phenylketonuria in Spain: RFLP haplotypes and linked mutations Lourdes R. DesviatBelén PérezMagdalena Ugarte Original Investigations Pages: 254 - 258
Human chromosome 11 complements ataxia-telangiectasia cells but does not complement the defect in AT-like Chinese hamster cell mutants W. JongmansJ. WiegantM. Z. Zdzienicka Original Investigations Pages: 259 - 264
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 NordvågIda RanløvM. Raafat El-Gewely Original Investigations Pages: 265 - 268
Founder effect in a Belgian-Dutch fragile X population Sonja BuyleEdwin ReyniersPatrick J. Willems Original Investigations Pages: 269 - 272
Genetic and molecular analysis of familial isolated growth hormone deficiency Rosalía Ruiz-PachecoPierre ChatelainCharles Sultan Original Investigations Pages: 273 - 281
Long range restriction map of the von Hippel-Lindau gene region on human chromosome 3p Susanne C. SzymanskiHolger HummerichElisabeth Schröder Original Investigations Pages: 282 - 288
Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis Hagit SerethTzipora ShoshaniBat-sheva Kerem Original Investigations Pages: 289 - 295
Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus Agneta NordenskjöldFredrik HedborgMagnus Nordenskjöld Short Communications Pages: 296 - 298
Genetic mapping of the erythropoietin receptor gene Pertti SistonenAnn-Liz TräskelinAlbert de la Chapelle Short Communications Pages: 299 - 301
Detection of an exon 53 polymorphism in the dystrophin gene Thomas W. PriorAudrey C. PappMary S. Sedra Short Communications Pages: 302 - 304
Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints R. J. SinkeB. de LeeuwA. Geurts van Kessel Short Communications Pages: 305 - 308
Fetal cells in the maternal circulation during first trimester in pregnancies Jui-Der LiouChia C. PaoShu-Min Kao Short Communications Pages: 309 - 311
Dinucleotide repeat polymorphisms at the lipoprotein lipase (LPL) locus T. M. NarcisiM. C. SchotzC. C. Shoulders OriginalPaper Pages: 312 - 313