Ordering markers in the region of the ataxia-telangiectasia gene (11q22-q23) by fluorescence in situ hybridization (FISH) to interphase nuclei Dorra CherifHera Der-SarkissianRoland Berger Original Investigations Pages: 1 - 6
Incidence of chromosome 3, 7, 10, 11, 17 and X disomy in mature human sperm nuclei as determined by nonradioactive in situ hybridization Martina GuttenbachRenate SchakowskiMichael Schmid Original Investigations Pages: 7 - 12
Human high-affinity FcγRI (CD64) gene mapped to chromosome 1q21.2-q21.3 by fluorescence in situ hybridization S. TakaiM. KasamaT. Taniyama Original Investigations Pages: 13 - 15
Quantification of point mutations associated with Leber hereditary optic neuroretinopathy by solid-phase minisequencing Vesa JuvonenKirsi HuoponenMarja-Liisa Savontaus Original Investigations Pages: 16 - 20
A human gene that restores the DNA-repair defect in SCID mice is located on 8p11.1→q11.1 Akihiro KurimasaYuiko NagataMitsuo Oshimura Original Investigations Pages: 21 - 26
Genetic analysis of the catalytic domain of the GAP gene in human lung cancer cell lines Tetsuya MitsudomiEitan FriedmanAdi F. Gazdar Original Investigations Pages: 27 - 31
Achievement of meiosis in XXY germ cells: study of 543 sperm karyotypes from an XY/XXY mosaic patient J. CozziE. ChevretB. Sèle Original Investigations Pages: 32 - 34
Expression of (cac)n/(gtg)n simple repetitive sequences in mRNA of human lymphocytes Cornelia EpplenJörg T. Epplen Original Investigations Pages: 35 - 41
Presence of an expressed β-tubulin gene (TUBB) in the HLA class I region may provide the genetic basis for HLA-linked microtubule dysfunction Armin VolzElisabeth WeissAndreas Ziegler Original Investigations Pages: 42 - 46
Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresis Xue-Fan GuFelix de RooijBernard Grandchamp Original Investigations Pages: 47 - 52
Molecular genetic investigations of the mechanism of tumourigenesis in von Hippel-Lindau disease: analysis of allele loss in VHL tumours Paul A. CrosseyKeith FosterEamonn R. Maher Original Investigations Pages: 53 - 58
Two new mutations in the porphobilinogen deaminase gene and a screening method using PCR amplification of specific alleles Gunnel LundinAnna WedellMaria Anvret Original Investigations Pages: 59 - 62
Isolation and characterization of the human genomic locus coding for the putative metastasis control gene nm23-H1 Steven DooleyThomas SeibCornelius Welter Original Investigations Pages: 63 - 66
Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutations Thilo DörkRainer FislageBurkhard Tümmler Original Investigations Pages: 67 - 73
Population screening of lactate dehydrogenase deficiencies in Fukuoka Prefecture in Japan and molecular characterization of three independent mutations in the lactate dehydrogenase-B(H) gene Masato MaekawaKayoko SudoTakashi Kanno Short Communications Pages: 74 - 76
The T→C mutation at position +96 of the untranslated region 3′ to the terminating codon of the β-globin gene is a rare polymorphism that does not cause a β-thalassemia as previously ascribed Vladimir DivokyErol BaysalTitus H. J. Huisman Short Communications Pages: 77 - 78
Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32 Jude FitzgibbonBinoy AppukuttanDavid M. Hunt Short Communications Pages: 79 - 80
Nonsense mutations at Arg-1947 in two cases of familial neurofibromatosis type 1 in Japanese Takahiko HoriuchiNobuaki HattaShigeru Fujita Short Communications Pages: 81 - 83
Detection of a MspI restriction fragment length polymorphism for the human sex hormone-binding globulin (SHBG) gene Marie-Claude VohlFrance T. DionneClaude Bouchard DNA Variants Pages: 84 - 84
Highly polymorphic repeat marker within the β-amyloid precursor protein gene Stefania ZappataMichael B. PetersenChristina Brahe DNA Variants Pages: 85 - 86
Corrections to the human mitochondrial ribosomal RNA sequences Toni R. PrezantJohn V. AgapianNathan Fischel-Ghodsian DNA Variants Pages: 87 - 88
Genetic mapping of two loci, DXS454 and DXS458, with respect to the X-linked agammaglobulinemia gene locus Mohammed ParkarRuth LoveringChristine Kinnon DNA Variants Pages: 89 - 90
Detection by the polymerase chain reaction of two polymorphisms in exon 14 of the human inter-α-trypsin inhibitor heavy chain H1 gene L. ThibervilleJ. BourguignonJ. P. Martin DNA Variants Pages: 91 - 92
