Sfoglia per Autore
Frequencies and types of chromosome abnormalities associated with human male infertility
1982-01-01 Zuffardi, Orsetta; Tiepolo, Luciano
Yq deletion in fetal syndrome
1982-01-01 Bozzola, Mauro; Scotta, Ms; Lorini, Renata; Zuffardi, Orsetta; De Giacomo, Costantino; Severi, Francesca
Duplication of the short arm of chromosome 9. Analysis of five cases.
1982-01-01 Cuoco, C; Gimelli, G; Pasquali, Francesco; Poloni, L; Zuffardi, Orsetta; Alicata, P; Battaglino, G; Bernardi, F; Cerone, R; Coltellessa, M; Ghidoni, A; Motta, S.
Correlation between testicular tissue and H-Y phenotype in intersex patients
1983-01-01 Muller, U; Mayerova, A; Debus, B; Fraccaro, Marco; Gilgenkrants, S; Glatzl, J; Madan, K; Pfeiffer, Ra; Prader, A; Zuffardi, Orsetta
Deficiency, transposition and duplication of one 15q rwegion may be alternatively associated with Prader-Willi (or similar) syndrome. Analysis of seven cases after varying ascertainment.
1983-01-01 Fraccaro, Marco; Zuffardi, Orsetta; Buhler, E; Schinzel, A; Simoni, G; Witkowski, R; Bonifaci, E; Caufin, D; Cignacco, G; Delendi, N; Gargantini, L; Losanowa, T; La Marca, L; Ulrich, E; Vigi, V.
A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosage
1984-01-01 Maraschio, Paola; Danesino, Cesare; LO CURTO, Francesco; Zuffardi, Orsetta; Dalla Fior, T; Pedrotti, D.
The Cd technique identifies a specidic structure to centromeric function
1984-01-01 Lambiase, Simonetta; Maraschio, Paola; Zuffardi, Orsetta
Dup(3)(p2----pter) in two families, including one infant with cyclopia.
1985-01-01 G., Gimelli; C., Cuoco; M., Lituania; M., Cordone; M., Aricò; E., Bianchi; P., Maraschio; Zuffardi, Orsetta
Indirect immunofluorescence of inactive centromere as indicator of centromeric function
1986-01-01 Peretti, D; Maraschio, Paola; Lambiase, Simonetta; LO CURTO, Francesco; Zuffardi, Orsetta
Different reaction of inactive centromeres to anticentromeric antibodies
1986-01-01 Danesino, Cesare; Lambiase, Simonetta; LO CURTO, Francesco; Maraschio, Paola; Minelli, Antonella; Peretti, D.; Zuffardi, Orsetta
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function
1986-01-01 Peretti, Diletta; Maraschio, Paola; Lambiase, Simonetta; LO CURTO, Francesco; Zuffardi, Orsetta
A new chromosome instability disorder
1986-01-01 Maraschio, Paola; Peretti, Diletta; Lambiase, Simonetta; LO CURTO, Francesco; Caufin, D.; Gargantini, L.; Minoli, Lorenzo; Zuffardi, Orsetta
Translocation X;13 in a patient with retinoblastoma
1987-01-01 Ponzio, G; Savin, E; Cattaneo, G; Ghiotti, Mp; Marra, A; Zuffardi, Orsetta; Danesino, Cesare
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia
1987-01-01 Zuffardi, Orsetta; Gargantini, L.; Lambiase, Simonetta; LO CURTO, Francesco; Maraschio, Paola; Ford, C. E.
Immunodeficiency, centromeric heterochromatin instability of chromosome 1, 9 and 16 and facial anomalies: the ICF syndrome.
1988-01-01 Maraschio, Paola; Zuffardi, Orsetta; Dalla Fior, T; Tiepolo, Luciano
A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosome 2;7 and 5;20
1988-01-01 Vivarelli, R; Zuffardi, Orsetta; Maraschio, Paola; Anichini, C; Scarinci, R.
Orign and clinical significance of inv dup(15)
1988-01-01 Maraschio, Paola; Cuoco, C; Gimelli, G; Zuffardi, Orsetta; Tiepolo, Luciano
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.
1989-01-01 Ballabio, A; Andria, G; Carrozzo, R; Persico, G; Bick, D; Campbell, L; Ropers, Hh; FERGUSON SMITH, Ma; Gimelli, G; Fraccaro, M; Maraschio, Paola; Zuffardi, Orsetta; Bardoni, B; Guioli, S; Camerino, Giovanna
Alternate centromere inactivation in a pseudodicentric (15;20) associated with a progressive neurological disorder
1989-01-01 Rivera, H; Zuffardi, Orsetta; Maraschio, Paola; Caiulo, A; Anichini, C; Scarinci, R; Vivarelli, R.
Evidence for human mitotic mutant with pleiotropic effect
1989-01-01 Papi, L; Montali, E; Marconi, G; Bigozzi, U; Maraschio, Paola; Zuffardi, Orsetta
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Frequencies and types of chromosome abnormalities associated with human male infertility | 1-gen-1982 | Zuffardi, Orsetta; Tiepolo, Luciano | |
Yq deletion in fetal syndrome | 1-gen-1982 | Bozzola, Mauro; Scotta, Ms; Lorini, Renata; Zuffardi, Orsetta; De Giacomo, Costantino; Severi, Francesca | |
Duplication of the short arm of chromosome 9. Analysis of five cases. | 1-gen-1982 | Cuoco, C; Gimelli, G; Pasquali, Francesco; Poloni, L; Zuffardi, Orsetta; Alicata, P; Battaglino, G; Bernardi, F; Cerone, R; Coltellessa, M; Ghidoni, A; Motta, S. | |
Correlation between testicular tissue and H-Y phenotype in intersex patients | 1-gen-1983 | Muller, U; Mayerova, A; Debus, B; Fraccaro, Marco; Gilgenkrants, S; Glatzl, J; Madan, K; Pfeiffer, Ra; Prader, A; Zuffardi, Orsetta | |
Deficiency, transposition and duplication of one 15q rwegion may be alternatively associated with Prader-Willi (or similar) syndrome. Analysis of seven cases after varying ascertainment. | 1-gen-1983 | Fraccaro, Marco; Zuffardi, Orsetta; Buhler, E; Schinzel, A; Simoni, G; Witkowski, R; Bonifaci, E; Caufin, D; Cignacco, G; Delendi, N; Gargantini, L; Losanowa, T; La Marca, L; Ulrich, E; Vigi, V. | |
A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosage | 1-gen-1984 | Maraschio, Paola; Danesino, Cesare; LO CURTO, Francesco; Zuffardi, Orsetta; Dalla Fior, T; Pedrotti, D. | |
The Cd technique identifies a specidic structure to centromeric function | 1-gen-1984 | Lambiase, Simonetta; Maraschio, Paola; Zuffardi, Orsetta | |
Dup(3)(p2----pter) in two families, including one infant with cyclopia. | 1-gen-1985 | G., Gimelli; C., Cuoco; M., Lituania; M., Cordone; M., Aricò; E., Bianchi; P., Maraschio; Zuffardi, Orsetta | |
Indirect immunofluorescence of inactive centromere as indicator of centromeric function | 1-gen-1986 | Peretti, D; Maraschio, Paola; Lambiase, Simonetta; LO CURTO, Francesco; Zuffardi, Orsetta | |
Different reaction of inactive centromeres to anticentromeric antibodies | 1-gen-1986 | Danesino, Cesare; Lambiase, Simonetta; LO CURTO, Francesco; Maraschio, Paola; Minelli, Antonella; Peretti, D.; Zuffardi, Orsetta | |
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function | 1-gen-1986 | Peretti, Diletta; Maraschio, Paola; Lambiase, Simonetta; LO CURTO, Francesco; Zuffardi, Orsetta | |
A new chromosome instability disorder | 1-gen-1986 | Maraschio, Paola; Peretti, Diletta; Lambiase, Simonetta; LO CURTO, Francesco; Caufin, D.; Gargantini, L.; Minoli, Lorenzo; Zuffardi, Orsetta | |
Translocation X;13 in a patient with retinoblastoma | 1-gen-1987 | Ponzio, G; Savin, E; Cattaneo, G; Ghiotti, Mp; Marra, A; Zuffardi, Orsetta; Danesino, Cesare | |
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia | 1-gen-1987 | Zuffardi, Orsetta; Gargantini, L.; Lambiase, Simonetta; LO CURTO, Francesco; Maraschio, Paola; Ford, C. E. | |
Immunodeficiency, centromeric heterochromatin instability of chromosome 1, 9 and 16 and facial anomalies: the ICF syndrome. | 1-gen-1988 | Maraschio, Paola; Zuffardi, Orsetta; Dalla Fior, T; Tiepolo, Luciano | |
A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosome 2;7 and 5;20 | 1-gen-1988 | Vivarelli, R; Zuffardi, Orsetta; Maraschio, Paola; Anichini, C; Scarinci, R. | |
Orign and clinical significance of inv dup(15) | 1-gen-1988 | Maraschio, Paola; Cuoco, C; Gimelli, G; Zuffardi, Orsetta; Tiepolo, Luciano | |
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome. | 1-gen-1989 | Ballabio, A; Andria, G; Carrozzo, R; Persico, G; Bick, D; Campbell, L; Ropers, Hh; FERGUSON SMITH, Ma; Gimelli, G; Fraccaro, M; Maraschio, Paola; Zuffardi, Orsetta; Bardoni, B; Guioli, S; Camerino, Giovanna | |
Alternate centromere inactivation in a pseudodicentric (15;20) associated with a progressive neurological disorder | 1-gen-1989 | Rivera, H; Zuffardi, Orsetta; Maraschio, Paola; Caiulo, A; Anichini, C; Scarinci, R; Vivarelli, R. | |
Evidence for human mitotic mutant with pleiotropic effect | 1-gen-1989 | Papi, L; Montali, E; Marconi, G; Bigozzi, U; Maraschio, Paola; Zuffardi, Orsetta |
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