Sfoglia per Autore
Prenatal diagnosis of the fragile-X in male monozygotic twins: discordant expression of the fragile site in amniocytes
1985-01-01 Rocchi, Mariano; Pecile, V; Archidiacono, Nicoletta; Monni, G; Dumez, Y; Filippi, G.
Cytologic demonstration of differential activity of rRNA gene clusters in different human tissues
1985-01-01 de Capoa, A; Marlekaj, P; Baldini, A; Rocchi, Mariano; Archidiacono, Nicoletta
Rett syndrome and fragile site in Xp22
1985-01-01 Archidiacono, Nicoletta; Rett, A; Rocchi, Mariano; Rolando, S; Lugaresi, E; Romeo, G.
Hormone-modulated rRNA gene activity is visualized by selective staining of the NOs.
1985-01-01 de Capoa, A; Baldini, A; Marlekaj, P; Natoli, C; Rocchi, Mariano; Archidiacono, Nicoletta; Cianfarani, S; Spadoni, Gl; Boscherini, B.
Mapping through somatic cell hybrids and cDNA probes of protein C to chromosome 2, factor X to chromosome 13, and alpha-1-acid glycoprotein to chromosome 9
1986-01-01 Rocchi, Mariano; Roncuzzi, L; Santamaria, R; Archidiacono, Nicoletta; Dente, L; Romeo, G.
Rett syndrome: lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations
1986-01-01 Romeo, G; Archidiacono, Nicoletta; Ferlini, A; Rocchi, Mariano
Growth hormone-induced regulation of rRNA gene activity in human cultured cells
1986-01-01 de Capoa, A; Marlekaj, P; Baldini, A; Felli, Mp; Rocchi, Mariano; Archidiacono, Nicoletta; Cianfarani, S; Spadoni, Gl; Boscherini, B.
X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families)
1987-01-01 Rocchi, Mariano; Archidiacono, Nicoletta; Filippi, G.
X-linked mental retardation. II. Renpenning syndrome and other types (report of 14 families)
1987-01-01 Archidiacono, Nicoletta; Rocchi, Mariano; Rinaldi, A; Filippi, G.
Nebulin and titin expression in Duchenne muscular dystrophy appears normal
1987-01-01 Fürst, D; Nave, R; Osborn, M; Weber, K; Bardosi, A; Archidiacono, Nicoletta; Ferro, M; Romano, V; Romeo, G.
Comparison of cytologic and genetic distances between long arm subtelomeric markers of human autosome 14 suggests uneven distribution of crossing-over
1987-01-01 Purrello, M; Alhadeff, B; Whittington, E; Buckton, Ke; Daniel, A; Arnaud, P; Rocchi, Mariano; Archidiacono, Nicoletta; Filippi, G; Siniscalco, M.
Italian experience regarding the prevention of Duchenne and Becker muscular dystrophies.
1988-01-01 Romeo, G; Devoto, M; Archidiacono, Nicoletta; Ferlini, A; Roncuzzi, L; Melis, Ma; Paderi, E; Ferrari, M; Tedeschi, S; Galluzzi, G.
Relationship between the number and function of human ribosomal genes
1988-01-01 de Capoa, A; Felli, Mp; Baldini, A; Rocchi, Mariano; Archidiacono, Nicoletta; Aleixandre, C; Miller, Oj; Miller, D. A.
Prevalence of mental retardation related to fragile X syndrome and other chromosomal abnormalities in the Republic of San Marino
1988-01-01 Cammarata, S; Archidiacono, Nicoletta; Romeo, G; Benassi, G; Guarino, M; D'Alessandro, R.
Physical dissection of the human X chromosome with special reference to the region Xq27-Xqter
1989-01-01 Rocchi, Mariano; Romeo, G; Giambarrasi, I; Castagnola, S; Archidiacono, Nicoletta
Autosomal dominant polycystic kidney disease: prenatal diagnosis by DNA analysis and sonography at 14 weeks.
1989-01-01 Ceccherini, I; Lituania, M; Cordone, Ms; Perfumo, F; Gusmano, R; Callea, F; Archidiacono, Nicoletta; Romeo, G.
Chromosome-specific subsets of human alphoid DNA identified by a chromosome 2-derived clone
1990-01-01 Rocchi, Mariano; Baldini, A; Archidiacono, Nicoletta; Lainwala, S; Miller, Oj; Miller, Da
Physical mapping of the human chromosome 11q23 region containing the ataxia-telangiectasia locus
1990-01-01 Wei, S; Rocchi, Mariano; Archidiacono, Nicoletta; Sacchi, N; Romeo, G; Gatti, Ra
A human alpha satellite DNA subset specific for chromosome 12
1990-01-01 Baldini, A; Rocchi, Mariano; Archidiacono, Nicoletta; Miller, Oj; Miller, Da
Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effect
1990-01-01 Rocchi, Mariano; Archidiacono, Nicoletta; Rinaldi, A; Filippi, G; Bartolucci, G; Fancello, Gs; Siniscalco, M.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Prenatal diagnosis of the fragile-X in male monozygotic twins: discordant expression of the fragile site in amniocytes | 1-gen-1985 | Rocchi, Mariano; Pecile, V; Archidiacono, Nicoletta; Monni, G; Dumez, Y; Filippi, G. | |
Cytologic demonstration of differential activity of rRNA gene clusters in different human tissues | 1-gen-1985 | de Capoa, A; Marlekaj, P; Baldini, A; Rocchi, Mariano; Archidiacono, Nicoletta | |
Rett syndrome and fragile site in Xp22 | 1-gen-1985 | Archidiacono, Nicoletta; Rett, A; Rocchi, Mariano; Rolando, S; Lugaresi, E; Romeo, G. | |
Hormone-modulated rRNA gene activity is visualized by selective staining of the NOs. | 1-gen-1985 | de Capoa, A; Baldini, A; Marlekaj, P; Natoli, C; Rocchi, Mariano; Archidiacono, Nicoletta; Cianfarani, S; Spadoni, Gl; Boscherini, B. | |
Mapping through somatic cell hybrids and cDNA probes of protein C to chromosome 2, factor X to chromosome 13, and alpha-1-acid glycoprotein to chromosome 9 | 1-gen-1986 | Rocchi, Mariano; Roncuzzi, L; Santamaria, R; Archidiacono, Nicoletta; Dente, L; Romeo, G. | |
Rett syndrome: lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations | 1-gen-1986 | Romeo, G; Archidiacono, Nicoletta; Ferlini, A; Rocchi, Mariano | |
Growth hormone-induced regulation of rRNA gene activity in human cultured cells | 1-gen-1986 | de Capoa, A; Marlekaj, P; Baldini, A; Felli, Mp; Rocchi, Mariano; Archidiacono, Nicoletta; Cianfarani, S; Spadoni, Gl; Boscherini, B. | |
X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families) | 1-gen-1987 | Rocchi, Mariano; Archidiacono, Nicoletta; Filippi, G. | |
X-linked mental retardation. II. Renpenning syndrome and other types (report of 14 families) | 1-gen-1987 | Archidiacono, Nicoletta; Rocchi, Mariano; Rinaldi, A; Filippi, G. | |
Nebulin and titin expression in Duchenne muscular dystrophy appears normal | 1-gen-1987 | Fürst, D; Nave, R; Osborn, M; Weber, K; Bardosi, A; Archidiacono, Nicoletta; Ferro, M; Romano, V; Romeo, G. | |
Comparison of cytologic and genetic distances between long arm subtelomeric markers of human autosome 14 suggests uneven distribution of crossing-over | 1-gen-1987 | Purrello, M; Alhadeff, B; Whittington, E; Buckton, Ke; Daniel, A; Arnaud, P; Rocchi, Mariano; Archidiacono, Nicoletta; Filippi, G; Siniscalco, M. | |
Italian experience regarding the prevention of Duchenne and Becker muscular dystrophies. | 1-gen-1988 | Romeo, G; Devoto, M; Archidiacono, Nicoletta; Ferlini, A; Roncuzzi, L; Melis, Ma; Paderi, E; Ferrari, M; Tedeschi, S; Galluzzi, G. | |
Relationship between the number and function of human ribosomal genes | 1-gen-1988 | de Capoa, A; Felli, Mp; Baldini, A; Rocchi, Mariano; Archidiacono, Nicoletta; Aleixandre, C; Miller, Oj; Miller, D. A. | |
Prevalence of mental retardation related to fragile X syndrome and other chromosomal abnormalities in the Republic of San Marino | 1-gen-1988 | Cammarata, S; Archidiacono, Nicoletta; Romeo, G; Benassi, G; Guarino, M; D'Alessandro, R. | |
Physical dissection of the human X chromosome with special reference to the region Xq27-Xqter | 1-gen-1989 | Rocchi, Mariano; Romeo, G; Giambarrasi, I; Castagnola, S; Archidiacono, Nicoletta | |
Autosomal dominant polycystic kidney disease: prenatal diagnosis by DNA analysis and sonography at 14 weeks. | 1-gen-1989 | Ceccherini, I; Lituania, M; Cordone, Ms; Perfumo, F; Gusmano, R; Callea, F; Archidiacono, Nicoletta; Romeo, G. | |
Chromosome-specific subsets of human alphoid DNA identified by a chromosome 2-derived clone | 1-gen-1990 | Rocchi, Mariano; Baldini, A; Archidiacono, Nicoletta; Lainwala, S; Miller, Oj; Miller, Da | |
Physical mapping of the human chromosome 11q23 region containing the ataxia-telangiectasia locus | 1-gen-1990 | Wei, S; Rocchi, Mariano; Archidiacono, Nicoletta; Sacchi, N; Romeo, G; Gatti, Ra | |
A human alpha satellite DNA subset specific for chromosome 12 | 1-gen-1990 | Baldini, A; Rocchi, Mariano; Archidiacono, Nicoletta; Miller, Oj; Miller, Da | |
Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effect | 1-gen-1990 | Rocchi, Mariano; Archidiacono, Nicoletta; Rinaldi, A; Filippi, G; Bartolucci, G; Fancello, Gs; Siniscalco, M. |
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