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Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-1989 Colour blindness (CB) distribution in the male population of Albanian and Croatian communities of Molise, Italy (with a review of the published Caucasoid CB gene frequencies). Malaspina, P; Biondi, G; Santillo, C Articolo su rivista
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 ON THE ESTIMATION OF THE AGE AT ONSET DISTRIBUTION IN HUNTINGTONS-CHOREA USING THE EM ALGORITHM Brambilla, C; Frontali, M; Malaspina, P; Rossi, C 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 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-1991 A further polymorphism of the Gd locus for glucose-6-phosphate dehydrogenase present among blacks (Nigerians) and apparently absent among caucasoids: The quantitative isoelectrophoretic variation of the Gd+ allele Modiano, G; Ciminelli, Bm; Malaspina, P; Santolamazza, P; Sedran, L; Meloni, T; Forteleoni, G; Mela, G Articolo su rivista
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 in vitro activity of the red cell glucose-6-phosphate dehydrogenase (G6PD) and the mch remain constant over long periods of time in healthy adult individuals because they depend only on their genome Modiano, G; Ciminelli, Bm; Malaspina, P; Parisi, P 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-1993 A cosmid library specific for human chromosome regions 6p23.1 and 6q27. Shortle, V; Malaspina, P; Fox, M; Dooley, J; Volz, A; Ziegler, A; Trowsdale, J; Morrison, K; Edwards, Y 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 EUROGEM map of human chromosome 14. Attwood, J; Kruse, T; Vergnaud, G; Malaspina, P; Povey, S 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
Mostrati risultati da 1 a 20 di 66
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