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| Genetic Policy |
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| European-wide opposition against the breast cancer gene patents FREE |
| Gert Matthijs & Dicky Halley |
| Abstract | Full text | PDF |
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| 783 |
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| Letter |
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| The significance of paired MEFV mutations in individuals without symptoms of familial Mediterranean fever FREE |
Mehmet Tunca, Servet Akar, Philip N Hawkins, Susanne E Booth, Bülent  engül, Tugba Ula Yavuzen, Selda Öktem, Müjde Soytürk, Nurullah Akkoç & David R Booth |
| Abstract | Full text | PDF |
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| 786 |
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| Articles |
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| Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements FREE |
| Heike Starke, Jörg Seidel, Wolfram Henn, Sylvia Reichardt, Marianne Volleth, Markus Stumm, Christine Behrend, Klaus R Sandig, Christine Kelbova, Gabriele Senger, Beate Albrecht, Ingo Hansmann, Anita Heller, Uwe Claussen & Thomas Liehr |
| Abstract | Full text | PDF |
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| 790 |
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| Meiotic outcomes in reciprocal translocation carriers ascertained in 3-day human embryos FREE |
| Caroline Mackie Ogilvie & Paul N Scriven |
| Abstract | Full text | PDF |
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| 801 |
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| Delineation of an estimated 6.7 MB candidate interval for an anophthalmia gene at 3q26.33-q28 and description of the syndrome associated with visible chromosome deletions of this region FREE |
| Alison Male, Angela Davies, Anne Bergbaum, Jean Keeling, David FitzPatrick, Caroline Mackie Ogilvie & Jonathan Berg |
| Abstract | Full text | PDF |
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| 807 |
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| Molecular and biochemical characterisation of a novel sulphatase gene: Arylsulfatase G (ARSG) FREE |
| Paola Ferrante, Silvia Messali, Germana Meroni & Andrea Ballabio |
| Abstract | Full text | PDF |
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| 813 |
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| Novel fibroblast growth factor receptor 3 (FGFR3) mutations in bladder cancer previously identified in non-lethal skeletal disorders FREE |
| Bas W G van Rhijn, Angela A G van Tilborg, Irene Lurkin, Jacky Bonaventure, Annie de Vries, Jean-Paul Thiery, Theodorus H van der Kwast, Ellen C Zwarthoff & Francois Radvanyi |
| Abstract | Full text | PDF |
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| 819 |
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| Clinical variability in calpainopathy: What makes the difference? FREE |
| Flávia de Paula, Mariz Vainzof, Maria Rita Passos-Bueno, Rita de Cássia M Pavanello, Sergio Russo Matioli, Louise V B Anderson, Vincenzo Nigro & Mayana Zatz |
| Abstract | Full text | PDF |
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| 825 |
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| New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile FREE |
| Myriam Ruault, Pierre van der Bruggen, Marie-Elisabeth Brun, Shelagh Boyle, Gérard Roizès & Albertina De Sario |
| Abstract | Full text | PDF |
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| 833 |
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| The importance of plasma apolipoprotein E concentration in addition to its common polymorphism on inter-individual variation in lipid levels: results from Apo Europe FREE |
| Nadia Haddy, Dirk De Bacquer, Marianne Mansour Chemaly, Mickaël Maurice, Christian Ehnholm, Alun Evans, Susanna Sans, Maria do Carmo Martins, Guy De Backer, Gérard Siest & Sophia Visvikis |
| Abstract | Full text | PDF |
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| 841 |
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| Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor FREE |
| Elise Chapiro, Delphine Feldmann, Françoise Denoyelle, Damien Sternberg, Claude Jardel, Marie-Madeleine Eliot, Didier Bouccara, Dominique Weil, Eréa-Noel Garabédian, Rémy Couderc, Christine Petit & Sandrine Marlin |
| Abstract | Full text | PDF |
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| 851 |
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| Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy FREE |
| Barry Chioza, Abena Osei-Lah, Lina Nashef, Blanca Suarez-Merino, Hazel Wilkie, Pak Sham, Jo Knight, Philip Asherson & Andrew J Makoff |
| Abstract | Full text | PDF |
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| 857 |
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| Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate FREE |
| Louise M Downey, T Jeffrey Keen, Ismail K Jalili, John McHale, Michael J Aldred, Steven P Robertson, Alan Mighell, Steven Fayle, Bernd Wissinger & Chris F Inglehearn |
| Abstract | Full text | PDF |
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| 865 |
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| Family-based association tests for quantitative traits using pooled DNA FREE |
| Joel S Bader & Pak Sham |
| Abstract | Full text | PDF |
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| 870 |
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| Short Reports |
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| BRCA2 founder mutation in Slovenian breast cancer families FREE |
| Mateja Krajc, Jacques De Grève, Guido Goelen & Erik Teugels |
| Abstract | Full text | PDF |
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| 879 |
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| Is DFNA5 a susceptibility gene for age-related hearing impairment? FREE |
| Lut Van Laer, Anita L DeStefano, Richard H Myers, Kris Flothmann, Sofie Thys, Erik Fransen, George A Gates, Guy Van Camp & Clinton T Baldwin |
| Abstract | Full text | PDF |
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| 883 |
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| Erratum |
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| De novo mutations in familial adenomatous polyposis (FAP) FREE |
| R Ripa, M L Bisgaard, S Bulow & F C Nielsen |
| Abstract | Full text | PDF |
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| 887 |
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| Author Index to Volume 10 |
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| Author Index to Volume 10 FREE |
| Abstract | Full text | PDF |
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| 889 |
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| Keyword Index to Volume 10 |
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| Keyword Index to Volume 10 FREE |
| Abstract | Full text | PDF |
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| 894 |
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| December 2002, Volume 10, Number 12 |
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