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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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