Telomere elongation observed in immortalized human fibroblasts by treatment with 60Co gamma rays or 4-nitroquinoline 1-oxide Shinsuke SugiharaKoichiro MiharaMasayoshi Namba Original Investigation Pages: 1 - 6
Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype Viviane DumurRadj GervaisPhilippe Roussel Original Investigation Pages: 7 - 10
Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A Rudy M. LandsvaterRumo P. M. JansenHans Kristian Ploos van Amstel Original Investigation Pages: 11 - 14
DMA polymorphisms in adhesion molecule genes — a new risk factor for early atherosclerosis Katrin WenzelMonika ErnstAstrid Speer Original Investigation Pages: 15 - 20
Direct detection of disomy in human sperm by the PRINS technique Franck PellestorIsabelle QuennessonJean Paul Charlieu Original Investigation Pages: 21 - 25
Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP) Vincent TimmermanAnn LöfgrenChristine Van Broeckhoven Original Investigation Pages: 26 - 34
A novel mutation in exon 17 of the β-subunit of rod phosphodiesterase in two RP sisters of a consanguineous family Diana ValverdeTeresa SolansMontserrat Baiget Original Investigation Pages: 35 - 38
Ullrich-Turner syndrome is not caused by haploinsufficiency of RPS4X Claudia GeerkensWalter JustWalther Vogel Original Investigation Pages: 39 - 44
Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal haemoglobinuria (PNH) patients Anna SavoiaLeonarda IanzanoLeopoldo Zelante Original Investigation Pages: 45 - 48
Mean corpuscular hemoglobin is not increased in Fmr1 knockout mice Edwin ReyniersDirk R. Van BockstaelePatrick J. Willems Original Investigation Pages: 49 - 50
Hereditary tyrosinemia type 1: novel missense, nonsense and splice consensus mutations in the human fumarylacetoacetate hydrolase gene; variability of the genotype-phenotype relationship J. K. Ploos van AmstelA. J. I. W. BergmanR. Berger Original Investigation Pages: 51 - 59
Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1 Dorothy TrumpGiuseppe PiliaRajesh V. Thakker Original Investigation Pages: 60 - 68
A clinical and molecular study of mosaicism for trisomy 17 Lisa G. ShafferChristopher McCaskillJames R. Lupski Original Investigation Pages: 69 - 72
Pseudohypoparathyroidism type Ia: two new heterozygous frameshift mutations in exons 5 and 10 of the Gsα gene Hagit ShapiraMeir MouallemZvi Farfel Original Investigation Pages: 73 - 75
Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophy M. ConnartyN. R. DennisJ. F. Harvey Original Investigation Pages: 76 - 78
Xp-duplications with and without sex reversal Annette BaumstarkGotthold BarbiWalter Just Original Investigation Pages: 79 - 86
A novel site of DNA amplification on chromosome 1p32-33 in a rhabdomyosarcoma revealed by comparative genomic hybridization Heike Steilen-GimbelKlaus RembergerWolfram Henn Original Investigation Pages: 87 - 90
Mutational analysis of the human cyclin-dependent kinase inhibitor p27kip1 in primary breast carcinomas Adolfo A. FerrandoMilagros BalbínCarlos López-Otín Original Investigation Pages: 91 - 94
Precise chromosomal locations of the genes for dentatorubral-pallidoluysian atrophy (DRPLA), von Willebrand factor (F8vWF) and parathyroid hormone-like hormone (PTHLH) in human chromosome 12p by deletion mapping Akira KuwanoYuji MorimotoIkuko Kondo Original Investigation Pages: 95 - 98
Apparent higher frequency of phenylketonuria in the Mexican state of Jalisco Antonio VelázquezGuadalupe BilbaoBetsy Phoenix Original Investigation Pages: 99 - 102
Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE) Gwenola GandonAnne Marie JouanolleJacqueline Yaouanq Original Investigation Pages: 103 - 113
Isolation and characterization of the human mismatch repair gene hMSH2 promoter region Stefan J. SchererThomas SeibCornelius Welter Original Investigation Pages: 114 - 116
Characterisation of a short interspersed repeat (Mermaid) that has family members on human chromosome 21 and elsewhere in the human genome J. HoyleI. G. YulugM. Fox Original Investigation Pages: 117 - 120
Identification of three neurofibromatosis type 2 (NF2) gene mutations in vestibular schwannomas Jesús SainzKarla FigueroaStefan-Matthias Pulst Short Communication Pages: 121 - 123
A highly polymorphic CA/GT repeat in intron 3 of the human urokinase receptor gene (PLAUR) Maija R. J. Kohonen-CorishYao WangWilliam F. Doe OriginalPaper Pages: 124 - 125
Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methods Hisashi KobayashiTara Cox MatiseEric P. Hoffman Erratum Pages: 126 - 126