Prospects for the genetics of human longevity François SchächterDaniel CohenTom Kirkwood Review Article Pages: 519 - 526
Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families: second locus or type I error? Ivona AksentijevichLuis GrubergDaniel L. Kastner Original Investigations Pages: 527 - 534
Localisation of the human nuclear factor I/X (NFI/X) gene to chromosome 19p13 and detection of five other related loci at 1p21-22, 1q42-43, 5q15, 11p13 and 20q13 by FISH C. SeisenbergerE. -L. WinnackerH. Scherthan Original Investigations Pages: 535 - 537
Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell lines Anna AlmeidaNadja Kokalj-VokacBernard Malfoy Original Investigations Pages: 538 - 546
Age-related nonrandom chromosomal abnormalities in human low-grade astrocytomas Gundula ThielTanka LozanovaRegine Witkowski Original Investigations Pages: 547 - 550
Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height Tsutomu OgataNobutake Matsuo Original Investigations Pages: 551 - 562
Polyploidies in abortion material decrease with maternal age Miriam NeuberHelga RehderEberhard Schwinger Original Investigations Pages: 563 - 566
Rapid detection of trisomy 21 by quantitative PCR Ferdinand von EggelingMichael FreytagUwe Claussen Original Investigations Pages: 567 - 570
New markers for linkage analysis of X-linked hypophosphataemic rickets P. S. N. RoweJ. GouldingJ. L. H. O'Riordan Original Investigations Pages: 571 - 575
Evidence for involvement of a second genetic locus on chromosome 11q in porphyrin metabolism B. NortonW. G. LanyonJ. M. Connor Original Investigations Pages: 576 - 578
Differential contribution of C4 and HLA-DQ genes to systemic lupus erythematosus susceptibility Dolores De JuanJosé M. Martín-VillaAntonio Arnaiz-Villena Original Investigations Pages: 579 - 584
Regional chromosomal assignment of the Kell blood group locus (KEL) to chromosome 7q33-q35 by fluorescence in situ hybridization: evidence for the polypeptide nature of antigenic variation Margo T. MurphyNorma MorrisonElizabeth Boyd Original Investigations Pages: 585 - 588
Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization Rina PlattnerNyla A. HeeremaCatherine G. Palmer Original Investigations Pages: 589 - 598
Exon skipping due to a mutation in a donor splice site in the WT-1 gene is associated with Wilms' tumor and severe genital malformations Susanne SchneiderGabi WildhardtBrigitte Royer-Pokora Original Investigations Pages: 599 - 604
Isolation and mapping of discrete DXS101 loci in Xq22 near the X-linked agammaglobulinaemia gene locus Marie-Anne J. O'ReillyAngela K. SweatmanChristine Kinnon Short Communications Pages: 605 - 608
Icelandic families with autosomal dominant polycystic kidney disease: families unlinked to chromosome 16p13.3 revealed by linkage analysis Ragnheiður FossdalMagnus BöðarssonÓlafur Jensson Short Communications Pages: 609 - 613
CF2603/4delT, a new frameshift mutation in exon 13 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene Begoña EzquietaJesús Molano OriginalPaper Pages: 614 - 615
A polymorphic CfoI site in exon 6 of the human cytochrome P450 CYP2D6 gene detected by the polymerase chain reaction Martin ArmstrongJeffrey R. IdleAnn K. Daly OriginalPaper Pages: 616 - 617
