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Mostrati risultati da 1 a 20 di 134
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-1990 The human Y chromosome shows a low level of DNA polymorphism Malaspina, P; Persichetti, F; Novelletto, A; Iodice, C; Terrenato, L; Wolfe, J; Ferraro, M; Prantera, G Articolo su rivista
1-gen-1990 Epidemiological and linkage studies on Huntington's disease in Italy Frontali, M; Malaspina, P; Rossi, C; Jacopini, A; Vivona, G; Pergola, M; Palena, A; Novelletto, A Articolo su rivista
1-gen-1990 An additional HindIII polymorphism at the coagulation factor XIIIA locus Iodice, C; Novelletto, A; Malaspina, P; Persichetti, F Articolo su rivista
1-gen-1991 Protection against malaria morbidity - near-fixation of the alpha-thalassemia gene in a Nepalese population Modiano, G; Morpurgo, G; Terrenato, L; Novelletto, A; Di Rienzo, A; Colombo, B; Purpura, M; Mariani, M; Santachiara Benerecetti, S; Brega, A; Dixit, K; Shrestha, S; Lania, A; Wanachiwanawin, W; Luzzatto, L Articolo su rivista
1-gen-1991 SPINOCEREBELLAR ATAXIA (SCA1) IN 2 LARGE ITALIAN KINDREDS - EVIDENCE IN FAVOR OF A LOCUS POSITION DISTAL TO GLO1 AND THE HLA CLUSTER Frontali, M; Iodice, C; Lulli, P; Spadaro, M; Cappellacci, S; Giunti, P; Malaspina, P; Morellini, M; Morocutti, C; Novelletto, A; Persichetti, F; Trabace, S; Anastasi, R; Terrenato, L Articolo su rivista
1-gen-1991 Linkage analysis and linkage disequilibrium studies between SCA1 and TG microsatellite VNTRs on 6p. Iodice, C; Persichetti, F; Frontali, M; Lulli, P; Spadaro, M; Cappellacci, S; Giunti, P; Malaspina, P; Morellini, M; Morocutti, C; Novelletto, A; Trabace, S; Terrenato, L Intervento a convegno
1-gen-1992 Disequilibrium of multiple DNA markers on the human Y chromosome Persichetti, F; Blasi, P; Hammer, M; Malaspina, P; Iodice, C; Terrenato, L; Novelletto, A Articolo su rivista
1-gen-1992 The Huntington's disease candidate region exhibits many different haplotypes Macdonald, Me; Novelletto, A; Lin, C; Tagle, D; Barnes, G; Bates, G; Taylor, S; Allitto, B; Altherr, M; Myers, R; Lehrach, H; Collins, Fs; Wasmuth, Jj; Frontali, M; Gusella, Jf Articolo su rivista
1-gen-1993 The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus Kwiatkowski, T; Orr, T; Banfi, S; Mccall, A; Iodice, C; Persichetti, F; Novelletto, A; Le Borgne De Marquois, F; Duvick, L; Frontali, M; Subramony, S; Beaudet, A; Terrenato, L; Zoghbi, H; Ranum, L Articolo su rivista
1-gen-1993 The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci Iodice, C; Frontali, M; Persichetti, F; Novelletto, A; Pandolfo, M; Spadaro, M; Giunti, P; Schinaia, G; Lulli, P; Malaspina, P; Plasmati, R; Tola, R; Antonelli, A; Di Donato, S; Morocutti, C; Weissenbach, J; Cann, Hm; Terrenato, L Articolo su rivista
1-gen-1994 Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I Iodice, C; Malaspina, P; Persichetti, F; Novelletto, A; Spadaro, M; Giunti, P; Morocutti, C; Terrenato, L; Harding, A; Frontali, M Articolo su rivista
1-gen-1994 The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias Giunti, P; Sweeney, M; Spadaro, M; Iodice, C; Novelletto, A; Malaspina, P; Frontali, M; Harding, A Articolo su rivista
1-gen-1994 The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias Giunti, P; Sweeney, M; Spadaro, M; Iodice, C; Novelletto, A; Malaspina, P; Frontali, M; Harding, A Articolo su rivista
1-gen-1995 Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulations Ciminelli, Bm; Pompei, F; Malaspina, P; Hammer, M; Persichetti, F; Pignatti, P; Palena, A; Anagnou, N; Guanti, G; Iodice, C; Terrenato, L; Novelletto, A Articolo su rivista
1-gen-1996 Genetic fitness in Huntington’s Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions. Frontali, M; Sabbadini, G; Novelletto, A; Iodice, C; Naso, F; Spadaro, M; Giunti, P; Jacopini, A; Veneziano, L; Mantuano, E; Malaspina, P; Ulizzi, L; Brice, A; Durr, A; Terrenato, L Articolo su rivista
1-gen-1996 Ordering of 44 genetic markers in the 6p22 cytogenetic band Trettel, F; Malaspina, P; Blasi, P; Iodice, C; Novelletto, A; Sabbadini, G; Veneziano, L; Frontali, M; Terrenato, L Articolo su rivista
1-gen-1996 Genetic fitness in Huntington's disease and spinocerebellar ataxia 1: A population genetics model for CAG repeat expansions Frontali, M; Sabbadini, G; Novelletto, A; Jodice, C; Naso, F; Spadaro, M; Giunti, P; Jacopini, A; Veneziano, L; Mantuano, E; Malaspina, P; Ulizzi, L; Brice, A; Durr, A; Terrenato, L Articolo su rivista
1-gen-1996 Construction of a YAC contig covering human chromosome 6p22 Malaspina, P; Roetto, A; Trettel, F; Iodice, C; Blasi, P; Frontali, M; Carella, M; Franco, B; Camaschella, C; Novelletto, A Articolo su rivista
1-gen-1996 Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats Rubinsztein, D; Leggo, J; Coles, R; Almqvist, E; Biancalana, V; Cassiman, J; Chotai, K; Connarty, M; Craufurd, D; Curtis, A; Curtis, D; Davidson, M; Differ, A; Dode, C; Dodge, A; Frontali, M; Ranen, N; Stine, O; Sherr, M; Abbott, M; Franz, M; Graham, C; Harper, P; Hedreen, J; Jackson, A; Kaplan, J; Losekoot, M; Macmillan, J; Morrison, P; Trottier, Y; Novelletto, A; Simpson, S; Theilmann, J; Whittaker, J; Folstein, S; Ross, C; Hayden, M Articolo su rivista
1-gen-1997 Differential structuring of human populations for homologous X and Y microsatellite loci Scozzari, R; Cruciani, F; Malaspina, P; Santolamazza, P; Ciminelli, Bm; Torroni, A; Modiano, D; Wallace, D; Kidd, K; Olckers, A; Moral, P; Terrenato, L; Akar, N; Qamar, R; Mansoor, A; Mehdi, S; Meloni, G; Vona, G; Cole, D; Cai, W; Novelletto, A Articolo su rivista
Mostrati risultati da 1 a 20 di 134
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