Determinants of the factor IX mutational spectrum in haemophilia B: an analysis of missense mutations using a multi-domain molecular model of the activated protein Adam I. WaceyMichael KrawczakDavid N. Cooper Original Investigation Pages: 594 - 608
Presence of chromosomal mosaicism in abnormal preimplantation embryos detected by fluorescence in situ hybridisation Edith CoonenJoyce C. HarperAlan H. Handyside Original Investigation Pages: 609 - 615
Location of the gene causing hyperimmunoglobulinemia D and periodic fever syndrome differs from that for familial mediterranean fever Joost P. H. DrenthEdwin C. M. MarimanInternational Hyper-IgD Study Group Original Investigation Pages: 616 - 620
The detection of mitochondrial DNA mutations using single stranded conformation polymorphism (SSCP) analysis and heteroduplex analysis Andrew Wyn ThomasRuth MorganJohn Alcolado Original Investigation Pages: 621 - 623
Physical mapping in the region of the Bruton's tyrosine kinase and α-galactosidase A gene loci in proximal Xq22 Angela K. SweatmanLinda A. D. BradleyChristine Kinnon Original Investigation Pages: 624 - 628
Complete detection of mutations in cystic fibrosis patients of Native American origin B. MercierO. RaguénèsC. Férec Original Investigation Pages: 629 - 632
Expression and chromosomal mapping of the gene encoding the human histone H1.1 P. BurfeindS. Hoyer-FenderW. Engel Original Investigation Pages: 633 - 639
Genetic heterogeneity of severe von Willebrand disease type III in the German population Reinhard SchneppenheimSonja KreyEva Simeoni Original Investigation Pages: 640 - 652
Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene Eva NelisVincent TimmermanChristine Van Broeckhoven Original Investigation Pages: 653 - 657
A WAGR region gene between PAX-6 and FSHB expressed in fetal brain Faina SchwartzRachael NeveGail Bruns Original Investigation Pages: 658 - 664
Oestrogen receptor (ESR) polymorphisms and breast cancer susceptibility Tone Ikdahl AndersonKetil Riddervold HeimdalAnne-Lise Børresen Original Investigation Pages: 665 - 670
The motilin gene: subregional localisation, tissue expression, DNA polymorphisms and exclusion as a candidate gene for the HLA-associated immotile cilia syndrome Paolo GaspariniAnna GrifaLeopoldo Zelante Original Investigation Pages: 671 - 674
The immunoglobulin heavy chain and disease association: application to pemphigus vulgaris William T. GibsonMichael A. WalterDiane W. Cox Original Investigation Pages: 675 - 683
New sites of methylcytosine-rich DNA detected on metaphase chromosomes Agnès BarbinClaire MontpellierClaire A. Bourgeois Original Investigation Pages: 684 - 692
Genetic heterogeneitiy of Crigler-Najjar syndrome type I: A study of 14 cases Philippe LabruneAnne MyaraMichel Odièvre Original Investigation Pages: 693 - 697
Exclusion of the cartilage link protein and the cartilage matrix protein genes as the mutant loci in several heritable chondrodysplasias John LoughlinCatherine IrvenBryan Sykes Short Communication Pages: 698 - 700
Male meiotic segregation of gonosomes analysed by two colour FISH in human interphase spermatozoa Edith ChevretSophie RousseauxBernard Sèle Short Communication Pages: 701 - 704
The human RAD51/RecA homologue gene is not a candidate gene for Bloom's syndrome Dennis HellgrenSigrid SahlénKerstin Kenne Short Communication Pages: 705 - 707
Exclusion of linkage with chromosome 21 in families with recurrence of non-Down's atrioventricular canal Massimo GennarelliGiuseppe NovelliBruno Dallapiccola Letter to the Editor Pages: 708 - 710