Anorexia nervosa viewed as an extreme weight condition: genetic implications Johannes HebebrandHelmut Remschmidt Review Article Pages: 1 - 11
Use of the primed in situ labelling (PRINS) technique for a rapid detection of chromosomes 13, 16, 18, 21, X and Y Franck PellestorAnne GirardetJean Paul Charlieu Original Investigation Pages: 12 - 17
Positional cloning of cDNAs from the human chromosome 3p21–22 region identifies a clustered organization of zinc-finger genes Viola CalabròGina PengueLuigi Lania Original Investigation Pages: 18 - 21
ANT3 and STS are autosomal in prosimian lemurs: implications for the evolution of the pseudoautosomal region Roland ToderGudrun A. RappoldWerner Schempp Original Investigation Pages: 22 - 28
Multi-PRINS: multiple sequential oligonucleotide primed in situ DNA synthesis reactions label specific chromosomes and produce bands E. J. M. SpeelDiane LawsonJohn Gosden Original Investigation Pages: 29 - 33
Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28 Michaela RathmannSusanna BungeAndreas Gal Original Investigation Pages: 34 - 38
Apolipoprotein E (apoE) polymorphism and its influence on ApoE concentrations in the cerebrospinal fluid in Finnish patients with Alzheimer's disease Terho LehtimäkiTuula PirttiläTapio Nikkari Original Investigation Pages: 39 - 42
Fluorescence in situ hybridisation studies provide evidence for somatic mosaicism in de novo dystrophin gene deletions David J. BunyanJohn A. CrollaDavid O. Robinson Original Investigation Pages: 43 - 45
High frequency of the apo ɛ4 allele in Khoi San from South Africa C. SandholzerRhena DelportG. Utermann Original Investigation Pages: 46 - 48
High resolution mid-prophase human chromosomes induced by echinomycin and ethidium bromide Jeffrey R. Sawyer Original Investigation Pages: 49 - 55
Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity E. C. M. MarimanS. E. C. van BeersumH. H. Ropers Original Investigation Pages: 56 - 62
XY gonadal dysgenesis and gonadoblastoma: a study in two sisters with a cryptic deletion of the Y chromosome involving the SRY gene Angela S. BarbosaThaís E. Ferraz-CostaCarlos A. Moreira-Filho Original Investigation Pages: 63 - 66
Linkage analysis in a Dutch family with X-linked recessive congenital stationary night blindness (XL-CSNB) Wolfgang BergerGerard van DuijnhovenFrans Cremers Original Investigation Pages: 67 - 70
Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family Rachel E. McGuireAlexandra M. GannonStephen P. Daiger Original Investigation Pages: 71 - 74
A topoisomerase II cleavage site is associated with a novel mitochondrial DNA deletion R. B. BlokD. R. ThorburnH.-H. M. Dahl Original Investigation Pages: 75 - 81
Isolation and characterization of a cosmid contig for the GCPS gene region Andrea VortkampChristiane HeidKarl-Heinz Grzeschik Original Investigation Pages: 82 - 88
Molecular analysis of the expression of transthyretin in intestine and liver from trisomy 18 fetuses Siobhan LoughnaPhillip BennettGudrun Moore Original Investigation Pages: 89 - 95
Assignment of the developmentally regulated gene NEDD1 to human chromosome 12q22 by fluorescence in situ hybridization S. TakaiY. YoshidaS. Kumar Short Communication Pages: 96 - 98
The human interleukin-10 receptor gene maps to chromosome 11q23.3 Tadayoshi TaniyamaSetsuo TakaiKiyomi Yamada Short Communication Pages: 99 - 101
Association between coronary heart disease and the apolipoprotein A-I/C-III/A-IV complex in a Japanese population Huai BaiKeijiro SakuKikuo Arakawa Short Communication Pages: 102 - 104
Novel mutation at the initiation codon in the Norrie disease gene in two Japanese families Yasushi IsashikiNorio OhbaNoriko Kuroda Short Communication Pages: 105 - 108
Characterization of a splicing mutation in the factor VIII gene at the RNA level Dezsö DavidAlice TavaresJoao Lavinha Short Communication Pages: 109 - 111
PKU in Slovakia: mutation screening and haplotype analysis Ludovit KádasiHelena PolákováVladimír Ferák Short Communication Pages: 112 - 114
Failure to detect Glut4-Ile383 and IR-Gln1152 variants in NIDDM (non-insulin dependent diabetes mellitus) and control subjects in an Italian population Laura EspositoPaola CarreraMaurizio Ferrari Short Communication Pages: 115 - 116
Trisomy 21 and maternal age of menopause: does reproductive age rather than chronological age influence risk of nondisjunction? Owen P. PhillipsShirley CromwellSherman Elias Short Communication Pages: 117 - 118
Five new microsatellite polymorphisms at the q21 region of human chromosome 21 Assumpció BoschStefan WiemannXavier Estivill Short Communication Pages: 119 - 122
A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome Barbara LüdeckeBernd DworniczakKlaus Bartholomé Clinical Case Report Pages: 123 - 125