Sfoglia per Autore
Acquisizioni Recenti Sulle Aberrazioni Costituzionali degli Autosomi
1983-01-01 Dallapiccola, B; Novelli, G; Palloni, R; Porfirio, B
La Citogenetica delle Sindromi Mieloproliferative
1983-01-01 Dallapiccola, B; Alimena, G; Novelli, G; Palloni, R; Gallo, E; De Cuia, Mr
Retrospective diagnosis of a Fanconi's anemia patient by dyepoxybutane (DEB) test results in parents
1983-01-01 Alimena, G; Avvisati, G; De Cuia, Mr; Gallo, E; Novelli, G; Dallapiccola, B
Pig red blood cell hexokinase: evidence for the presence of hexokinase types II and III, and their purification and characterization
1983-10-01 Stocchi, V; Magnani, M; Novelli, G; Dachà, M; Fornaini, G
Regional mapping of hexokinase-1 within the short arm of chromosome 10
1984-01-01 Dallapiccola, B; Novelli, G; Micara, G; Delaroche, I; Moric-Petrovic, S; Magnani, M
Hereditary nonspherocytic hemolytic anemia due to a new hexokinase variant with reduced stability
1985-09-01 Magnani, M; Stocchi, V; Cucchiarini, L; Novelli, G; Lodi, S; Isa, L; Fornaini, G
Analysis of isoenzymes in trophoblast cells
1986-01-01 Novelli, G; Catizone, F; Dallapiccola, B
Genetica Medica Essenziale
1988-01-01 Dallapiccola, B; Novelli, G
Gene dosage studies regionally assign the phosphoserine phosphatase gene to 7p15.1 or 2
1988-01-01 Novelli, G; Dallapiccola, B
Multilocus analysis of the fragile X syndrome
1988-03-01 Brown, Wt; Gross, A; Chan, C; Jenkins, Ec; Mandel, Jl; Oberlé, I; Arveiler, B; Novelli, G; Thibodeau, S; Hagerman, R
Deletion 2q31.3----2q33.3: gene dosage effect of ribulose 5-phosphate 3-epimerase
1988-05-01 Dallapiccola, B; Novelli, G; Giannotti, A
Protocol for prenatal diagnosis of cystic fibrosis based on studies of alkaline phosphatase isoenzymes
1988-08-01 Novelli, G; Mannello, F; Pierotti, C; Antonelli, M; Dallapiccola, B
DNA MarkersAnalysis of Adult Polycystic Kidney Disease in Italian Families
1989-01-01 Potenza, L; Mandich, P; Restagno, G; Bellone, E; Novelli, G; Dallapiccola, B; Ajmar, F; Carbonara, A
Textbook of Human Genetics
1989-01-01 Novelli, G
PCR amplification and silver stain detection of genomic DNA fragments
1989-09-01 Novelli, G; Mannello, F; Dallapiccola, B
Regional distribution of Cystic fibrosis linked DNA haplotypes in Italy, a collaborative study
1990-04-01 Gasparini, P; Cappello, N; Dallapiccola, B; Devoto, M; Estivill, X; Ferrari, M; Leoni, G; Novelli, G; Piazza, A; Pignatti, Pf; Romeo, G; Rosatelli, C; Savoia, A; Seia, M; Williamson, R
Delta F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish families
1990-06-01 Novelli, G; Sangiuolo, Fc; Dallapiccola, B; Gasparini, P; Savoia, A; Pignatti, P; Fernandez, E; Benitez, J; Casals, T; Nunes, V
Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF families
1990-09-01 Novelli, G; Gasparini, P; Savoia, A; Pignatti, P; Sangiuolo, Fc; Dallapiccola, B
Difetti Congeniti: Nosologia, Eziologia e Prevenzione
1991-01-01 Dallapiccola, B; Novelli, G
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms
1991-01-01 Gasparini, P; Mandich, P; Novelli, G; Bellone, E; Sangiuolo, Fc; De Stefano, F; Potenza, L; Trabetti, E; Marigo, M; Pignatti, P
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
1-gen-1983 | Acquisizioni Recenti Sulle Aberrazioni Costituzionali degli Autosomi | Dallapiccola, B; Novelli, G; Palloni, R; Porfirio, B | Articolo su rivista | |
1-gen-1983 | La Citogenetica delle Sindromi Mieloproliferative | Dallapiccola, B; Alimena, G; Novelli, G; Palloni, R; Gallo, E; De Cuia, Mr | Articolo su rivista | |
1-gen-1983 | Retrospective diagnosis of a Fanconi's anemia patient by dyepoxybutane (DEB) test results in parents | Alimena, G; Avvisati, G; De Cuia, Mr; Gallo, E; Novelli, G; Dallapiccola, B | Articolo su rivista | |
1-ott-1983 | Pig red blood cell hexokinase: evidence for the presence of hexokinase types II and III, and their purification and characterization | Stocchi, V; Magnani, M; Novelli, G; Dachà, M; Fornaini, G | Articolo su rivista | |
1-gen-1984 | Regional mapping of hexokinase-1 within the short arm of chromosome 10 | Dallapiccola, B; Novelli, G; Micara, G; Delaroche, I; Moric-Petrovic, S; Magnani, M | Articolo su rivista | |
1-set-1985 | Hereditary nonspherocytic hemolytic anemia due to a new hexokinase variant with reduced stability | Magnani, M; Stocchi, V; Cucchiarini, L; Novelli, G; Lodi, S; Isa, L; Fornaini, G | Articolo su rivista | |
1-gen-1986 | Analysis of isoenzymes in trophoblast cells | Novelli, G; Catizone, F; Dallapiccola, B | Articolo su rivista | |
1-gen-1988 | Genetica Medica Essenziale | Dallapiccola, B; Novelli, G | Monografia | |
1-gen-1988 | Gene dosage studies regionally assign the phosphoserine phosphatase gene to 7p15.1 or 2 | Novelli, G; Dallapiccola, B | Articolo su rivista | |
1-mar-1988 | Multilocus analysis of the fragile X syndrome | Brown, Wt; Gross, A; Chan, C; Jenkins, Ec; Mandel, Jl; Oberlé, I; Arveiler, B; Novelli, G; Thibodeau, S; Hagerman, R | Articolo su rivista | |
1-mag-1988 | Deletion 2q31.3----2q33.3: gene dosage effect of ribulose 5-phosphate 3-epimerase | Dallapiccola, B; Novelli, G; Giannotti, A | Articolo su rivista | |
1-ago-1988 | Protocol for prenatal diagnosis of cystic fibrosis based on studies of alkaline phosphatase isoenzymes | Novelli, G; Mannello, F; Pierotti, C; Antonelli, M; Dallapiccola, B | Articolo su rivista | |
1-gen-1989 | DNA MarkersAnalysis of Adult Polycystic Kidney Disease in Italian Families | Potenza, L; Mandich, P; Restagno, G; Bellone, E; Novelli, G; Dallapiccola, B; Ajmar, F; Carbonara, A | Contributo in libro | |
1-gen-1989 | Textbook of Human Genetics | Novelli, G | Articolo su rivista | |
1-set-1989 | PCR amplification and silver stain detection of genomic DNA fragments | Novelli, G; Mannello, F; Dallapiccola, B | Articolo su rivista | |
1-apr-1990 | Regional distribution of Cystic fibrosis linked DNA haplotypes in Italy, a collaborative study | Gasparini, P; Cappello, N; Dallapiccola, B; Devoto, M; Estivill, X; Ferrari, M; Leoni, G; Novelli, G; Piazza, A; Pignatti, Pf; Romeo, G; Rosatelli, C; Savoia, A; Seia, M; Williamson, R | Articolo su rivista | |
1-giu-1990 | Delta F508 gene deletion and prenatal diagnosis of cystic fibrosis in Italian and Spanish families | Novelli, G; Sangiuolo, Fc; Dallapiccola, B; Gasparini, P; Savoia, A; Pignatti, P; Fernandez, E; Benitez, J; Casals, T; Nunes, V | Articolo su rivista | |
1-set-1990 | Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF families | Novelli, G; Gasparini, P; Savoia, A; Pignatti, P; Sangiuolo, Fc; Dallapiccola, B | Articolo su rivista | |
1-gen-1991 | Difetti Congeniti: Nosologia, Eziologia e Prevenzione | Dallapiccola, B; Novelli, G | Contributo in libro | |
1-gen-1991 | Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphisms | Gasparini, P; Mandich, P; Novelli, G; Bellone, E; Sangiuolo, Fc; De Stefano, F; Potenza, L; Trabetti, E; Marigo, M; Pignatti, P | Articolo su rivista |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile