Hereditary cystatin C amyloid angiopathy: identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysis Magnus AbrahamsonSif JonsdottirAnders Grubb Original Investigations Pages: 377 - 380
Genetic heterogeneity of early-onset familial breast cancer Hagay SobolSylvie MazoyerDominique Guerin Original Investigations Pages: 381 - 383
Differences in apolipoprotein(a) polymorphism in West Greenland Eskimos and Caucasian Danes Ib Christian KlausenLars Ulrik GerdesOle Faergeman Original Investigations Pages: 384 - 388
Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts L. RoewerJ. AmemannJ. T. Epplen Original Investigations Pages: 389 - 394
Mutation analysis and prenatal diagnosis in a Lesch-Nyhan family showing non-random X-inactivation interfering with carrier detection tests Suzanne MarcusAnn-Marie SteenUta Francke Original Investigations Pages: 395 - 400
Molecular analysis of the gene for the human vitamin-D-binding protein (group-specific component): allelic differences of the common genetic GC types Andreas BraunRegina BichlmaierHartwig Cleve Original Investigations Pages: 401 - 406
Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis Kathelijne MangelschotsBernadette Van RoyPatrick J. Willems Original Investigations Pages: 407 - 413
A single base mutation in the gene for type III collagen (COL3A1) converts glycine 847 to glutamic acid in a family with Ehlers-Danlos syndrome type IV. An unaffected family member is mosaic for the mutation A. J. RichardsP. N. WardF. M. Pope Original Investigations Pages: 414 - 418
Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec Louise R. SimardFrance GingrasDamian Labuda Original Investigations Pages: 419 - 424
The segregation of a translocation t(1;4) in two male carriers heterozygous for the translocation A. M. EstopF. LevinsonV. Vankirk Original Investigations Pages: 425 - 429
Structural gene aberrations in mucopolysaccharidosis II (Hunter) Manfred WehnertJohn J. HopwoodFalko H. Herrmann Original Investigations Pages: 430 - 432
Familial pericentric inversion (3)(p12q24) Laura LindbergKia PeltoGeorg H. Borgström Original Investigations Pages: 433 - 436
Frequency of ΔF508 and haplotype association in Austrian cystic fibrosis families K. WagnerM. ZachW. Rosenkranz Original Investigations Pages: 437 - 438
Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata — a complementation study Judith C. HeikoopRonald J. A. WandersJoseph M. Tager Original Investigations Pages: 439 - 444
Loss of heterozygosity on chromosome 11 in sporadic gastrinomas Mark P. SawickiYu-Jui Yvonne WanEdward Passaro Jr Original Investigations Pages: 445 - 449
Paracentric inversion 11q in Canadian Hutterites B. N. ChodirkerC. R. GreenbergA. E. Chudley Original Investigations Pages: 450 - 452
Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus Ewa ZiÇetkiewiczDaniel SinnettDamian Labuda Short Communications Pages: 453 - 456
The Kell blood group locus is close to the cystic fibrosis locus on chromosome 7 Kavita R. PurohitJames L. WeberBronya J. B. Keats Short Communications Pages: 457 - 458
Molecular diagnosis of the transthyretin (TTR) Met111 mutation in familial amyloid cardiomyopathy of Danish origin Bjørn-Yngvar NordvågGunnar HusbyM. Raafat El-Gewely Short Communications Pages: 459 - 461
Consanguinity and Down syndrome in the Shetland Islands Ernest B. Hook Letters to the Editors Pages: 462 - 462
Data on the interaction of ABO blood groups and the haptoglobin system B. Rex-Kiss Letters to the Editors Pages: 463 - 463
Frequency of ΔF508 mutation and haplotype analysis in Austrian cystic fibrosis families Jörg LarsenAnthi GeorghiouJürgen Spona Letters to the Editors Pages: 464 - 465
A point mutation changes the polymorphisms pattern in a cystic fibrosis carrier family E. FernándezA. SantónJ. Benitez Letters to the Editors Pages: 465 - 466
