Sfoglia per Rivista
Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure
2000-01-01 Marozzi, A; Manfredini, E; Tibiletti, Mg; Furlan, Daniela; Villa, N; Vegetti, W; Crosignani, Pg; Ginelli, E; Meneveri, R; Dalpra, L.
Partial trisomy 1 due to 1/17 translocation in Ph'-positive Chronic Myelocytic leukemia
1979-01-01 Pasquali, Francesco; Francesconi, D.; Casalone, R.; Ippoliti, G.
Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases
1982-01-01 Pasquali, Francesco; Bernasconi, P.; Casalone, R.; Fraccaro, M.; Bernasconi, C.; Lazzarino, M.; Morra, E.; Alessandrino, E. P.; Marchi, M. A.; Sanger, R.
Shortdirect repeats at the breakpoints of a novel large deletion in the CFTR genesuggest a likely slipped mispairing mechanism
1996-01-01 Magnani, C; Cremonesi, L; Giunta, A; Magnaghi, P; Taramelli, Roberto; Ferrari, M.
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families
1983-01-01 Iselius, L.; Lindsten, J.; Aurias, A.; Fraccaro, M.; Pasquali, Francesco
The 11q;22q translocation: a european collaborative analysis of 43 cases
1980-01-01 Fraccaro, M.; Lindsten, J.; Ford, C.; Iselius, L.; Pasquali, Francesco
The isochromosome (17q) in chronic myelocytic leukaemia: mechanism of origin, centromeric function and clonal evolution
1982-01-01 Pasquali, Francesco; Panarello, C.; Bernasconi, P.; Casalone, R.
The origin and phenotype of X0 males
1987-01-01 Fraccaro, M; Lindsten, J; LO CURTO, Francesco
The Turner phenotype and the different types of human X isochromosome.
1982-01-01 Larizza, D.; Abbati, G.; Lorini, R.; Salvatoni, Alessandro; Severi, F.
Three chromosomes' (7;9;22) rearrangement and the origin of the Philadelphia chromosome
1978-01-01 Francesconi, D.; Pasquali, Francesco
Transposition of 9q34 and 22 (q11-qter) regions has a specific role in chronic myelocytic leukemia
1979-01-01 Pasquali, Francesco; Casalone, R.; Francesconi, D.; Peretti, D.; Fraccaro, M.; Bernasconi, C.; Lazzarino, M.
Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase
1988-01-01 Maserati, Emanuela; Cavalli, P.; Casalone, R.; Morandi, S.; Pasquali, Francesco
Type I procollagen in the severe non-lethal form of osteogenesis imperfecta.
1988-01-01 Tenni, R.; Cetta, G.; Dyne, K.; Rossi, A.; Quacci, DANIELA ELENA; Lenzi, L; Castellani, A. A.
Women heterozygous for deficiency of the (p21-pter) region of the X chromosome are fertile
1977-01-01 Fraccaro, M.; Maraschio, P.; Pasquali, Francesco; Scappaticci, S.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure | 1-gen-2000 | Marozzi, A; Manfredini, E; Tibiletti, Mg; Furlan, Daniela; Villa, N; Vegetti, W; Crosignani, Pg; Ginelli, E; Meneveri, R; Dalpra, L. | |
| Partial trisomy 1 due to 1/17 translocation in Ph'-positive Chronic Myelocytic leukemia | 1-gen-1979 | Pasquali, Francesco; Francesconi, D.; Casalone, R.; Ippoliti, G. | |
| Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases | 1-gen-1982 | Pasquali, Francesco; Bernasconi, P.; Casalone, R.; Fraccaro, M.; Bernasconi, C.; Lazzarino, M.; Morra, E.; Alessandrino, E. P.; Marchi, M. A.; Sanger, R. | |
| Shortdirect repeats at the breakpoints of a novel large deletion in the CFTR genesuggest a likely slipped mispairing mechanism | 1-gen-1996 | Magnani, C; Cremonesi, L; Giunta, A; Magnaghi, P; Taramelli, Roberto; Ferrari, M. | |
| The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families | 1-gen-1983 | Iselius, L.; Lindsten, J.; Aurias, A.; Fraccaro, M.; Pasquali, Francesco | |
| The 11q;22q translocation: a european collaborative analysis of 43 cases | 1-gen-1980 | Fraccaro, M.; Lindsten, J.; Ford, C.; Iselius, L.; Pasquali, Francesco | |
| The isochromosome (17q) in chronic myelocytic leukaemia: mechanism of origin, centromeric function and clonal evolution | 1-gen-1982 | Pasquali, Francesco; Panarello, C.; Bernasconi, P.; Casalone, R. | |
| The origin and phenotype of X0 males | 1-gen-1987 | Fraccaro, M; Lindsten, J; LO CURTO, Francesco | |
| The Turner phenotype and the different types of human X isochromosome. | 1-gen-1982 | Larizza, D.; Abbati, G.; Lorini, R.; Salvatoni, Alessandro; Severi, F. | |
| Three chromosomes' (7;9;22) rearrangement and the origin of the Philadelphia chromosome | 1-gen-1978 | Francesconi, D.; Pasquali, Francesco | |
| Transposition of 9q34 and 22 (q11-qter) regions has a specific role in chronic myelocytic leukemia | 1-gen-1979 | Pasquali, Francesco; Casalone, R.; Francesconi, D.; Peretti, D.; Fraccaro, M.; Bernasconi, C.; Lazzarino, M. | |
| Transposition of c–abl oncogene in a case of masked Ph chromosome duplicated in blastic phase | 1-gen-1988 | Maserati, Emanuela; Cavalli, P.; Casalone, R.; Morandi, S.; Pasquali, Francesco | |
| Type I procollagen in the severe non-lethal form of osteogenesis imperfecta. | 1-gen-1988 | Tenni, R.; Cetta, G.; Dyne, K.; Rossi, A.; Quacci, DANIELA ELENA; Lenzi, L; Castellani, A. A. | |
| Women heterozygous for deficiency of the (p21-pter) region of the X chromosome are fertile | 1-gen-1977 | Fraccaro, M.; Maraschio, P.; Pasquali, Francesco; Scappaticci, S. |
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