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Journal Abstract Search
127 related items for PubMed ID: 2016094
1. Localization of DNA probes tightly linked to the Friedreich's ataxia locus by in situ hybridization in a case of pericentric inversion of chromosome 9. Raimondi E, Bernasconi P, Moralli D, Fujita R, Uziel G, Di Donato S, De Carli L, Pandolfo M. Hum Genet; 1991 Mar; 86(5):525-8. PubMed ID: 2016094 [Abstract] [Full Text] [Related]
2. The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15. Hanauer A, Chery M, Fujita R, Driesel AJ, Gilgenkrantz S, Mandel JL. Am J Hum Genet; 1990 Jan; 46(1):133-7. PubMed ID: 2294745 [Abstract] [Full Text] [Related]
3. Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxia. Fujita R, Hanauer A, Sirugo G, Heilig R, Mandel JL. Proc Natl Acad Sci U S A; 1990 Mar; 87(5):1796-800. PubMed ID: 1968638 [Abstract] [Full Text] [Related]
4. Friedreich ataxia in Italian families: genetic homogeneity and linkage disequilibrium with the marker loci D9S5 and D9S15. Pandolfo M, Sirugo G, Antonelli A, Weitnauer L, Ferretti L, Leone M, Dones I, Cerino A, Fujita R, Hanauer A. Am J Hum Genet; 1990 Aug; 47(2):228-35. PubMed ID: 2378348 [Abstract] [Full Text] [Related]
5. Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q. Chamberlain S, Farrall M, Shaw J, Wilkes D, Carvajal J, Hillerman R, Doudney K, Harding AE, Williamson R, Sirugo G. Am J Hum Genet; 1993 Jan; 52(1):99-109. PubMed ID: 8434613 [Abstract] [Full Text] [Related]
6. Regional localization by in situ hybridization of a human chromosome 9 marker tightly linked to the Friedreich's ataxia locus. Raimondi E, Antonelli A, Driesel AJ, Pandolfo M. Hum Genet; 1990 Jun; 85(1):125-6. PubMed ID: 1972693 [Abstract] [Full Text] [Related]
7. Physical evidence for the position of the Friedreich's ataxia locus FRDA proximal to D9S5. Hillermann R, See CG, Pook M, Wilkes D, Carvajal J, Doudney K, Williamson R, Chamberlain S. Cytogenet Cell Genet; 1995 Jun; 71(3):214-6. PubMed ID: 7587379 [Abstract] [Full Text] [Related]
8. Friedreich's disease. A linkage study in southern and central Italy. Cavalcanti F, Cocozza S, Filla A, De Michele G, Pianese L, Porcellini A, Monticelli A, Pandolfo M, Banfi S, Varrone S. Acta Neurol (Napoli); 1992 Jun; 14(4-6):519-23. PubMed ID: 1363458 [Abstract] [Full Text] [Related]
9. A 530kb YAC contig tightly linked to the Friedreich ataxia locus contains five CpG clusters and a new highly polymorphic microsatellite. Fujita R, Sirugo G, Duclos F, Abderrahim H, Le Paslier D, Cohen D, Brownstein BH, Schlessinger D, Mandel JL, Koenig M. Hum Genet; 1992 Jul; 89(5):531-8. PubMed ID: 1353054 [Abstract] [Full Text] [Related]
10. Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresis. Fujita R, Hanauer A, Vincent A, Mandel JL, Koenig M. Genomics; 1991 Aug; 10(4):915-20. PubMed ID: 1916823 [Abstract] [Full Text] [Related]
11. Allele frequencies of DNA markers genetically linked to Friedreich ataxia in the German population. Zühlke C, Thies U. Hum Hered; 1993 Aug; 43(2):78-81. PubMed ID: 8103037 [Abstract] [Full Text] [Related]
18. Gene in the region of the Friedreich ataxia locus encodes a putative transmembrane protein expressed in the nervous system. Duclos F, Boschert U, Sirugo G, Mandel JL, Hen R, Koenig M. Proc Natl Acad Sci U S A; 1993 Jan 01; 90(1):109-13. PubMed ID: 7678331 [Abstract] [Full Text] [Related]
19. Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population. Pianese L, Cocozza S, Campanella G, Castaldo I, Cavalcanti F, De Michele G, Filla A, Monticelli A, Munaro M, Redolfi E. J Med Genet; 1994 Feb 01; 31(2):133-5. PubMed ID: 8182719 [Abstract] [Full Text] [Related]
20. Mapping of Friedreich's ataxia locus by identification of recombination events in patients homozygous by descent. Monrós E, Smeyers P, Rodius F, Cañizares J, Moltó MD, Vilchez JJ, Pandolfo M, Lopez-Arlandis J, de Frutos R, Prieto F. Eur J Hum Genet; 1994 Feb 01; 2(4):291-9. PubMed ID: 7704559 [Abstract] [Full Text] [Related] Page: [Next] [New Search]