Sfoglia per Autore
Reduced phenotypic effetc of partial trisomy 1q in a X/1 translocation.
1977-01-01 Zuffardi, Orsetta; Tiepolo, Luciano; Scappaticci, S; Francesconi, D; Bianchi, C; Di Natale, B.
"Cri du chat" syndrome due to a complex rearrangement of chromosome 5
1978-01-01 Francesconi, D; Zuffardi, Orsetta; D'Attoma, G; Fraccaro, Marco
BSu restriction of DNA from cases exhibiting sex chromosom abnormalities.
1978-01-01 Kinross, J; Fraccaro, Marco; Scappaticci, MARIA ASSUNTA; Tiepolo, Luciano; Zuffardi, Orsetta; Pawlowitzki, Ih; Jones, Kw
Chromosome 15 and Prader-Willi syndrome
1978-01-01 Zuffardi, Orsetta; Buhler, Em; Fraccaro, Marco
Five unusual karyotypes in Down's syndrome
1979-01-01 Csalone, R; Fraccaro, Marco; Francesconi, D; Pasquali, Francesco; Poloni, L; Zuffardi, Orsetta; Bellomi, A; Crosti, N; Lo Monaco, Gb; Patriarca, Pl; Serventi, M.
Familial XX true hermaphroditism and the H-Y antigen.
1979-01-01 Fraccaro, Marco; Tiepolo, Luciano; Zuffardi, Orsetta; Chiumello, G; Di Natale, B; Gargantini, L; Wolf, U.
Ring chromosome 12 and latent centromeres
1980-01-01 Zuffardi, Orsetta; Danesino, Cesare; Poloni, L; Pavesi, F; Bianchi, C; Gargantini, L.
Trisomy 16q21-->qter
1980-01-01 Garau, A; Crisponi, G; Peretti, D; Vanni, R; Zuffardi, Orsetta
Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223.
1980-01-01 Tiepolo, Luciano; Zuffardi, Orsetta; Fraccaro, Marco; Di Natale, B; Gargantini, L; Muller, Cr; Ropers, Hh
Turner syndrome patients are H-Y positive.
1980-01-01 Wolf, U; Fraccaro, Marco; Mayerova, A; Hecht, T; Zuffardi, Orsetta
Cd bands and centromeric function in dicentric chromosomes
1980-01-01 Maraschio, Paola; Zuffardi, Orsetta; LO CURTO, Francesco
A family group with four cases of Kartagener's syndrome
1980-01-01 Zuffardi, Orsetta; Zanon, P; Calligaro, A.
Xp deficiencies and female fertility
1980-01-01 Maraschio, Paola; Paquali, F; Zuffardi, Orsetta; Fraccaro, Marco
Ribosomal RNA in infertile male carriers of Robertsonian translocations
1980-01-01 Guanti, G; Zuffardi, Orsetta; Tiepolo, Luciano
The "cat eye syndrome": dicentric small marker chromosome probably derived from a n. 22 (tetrasomy 22pter-->q11) associated with a characteristic phenotype.
1981-01-01 Schinzel, A; Schmid, W; Fraccaro, Marco; Tiepolo, Luciano; Zuffardi, Orsetta; Opitz, Jm; Lindsten, J; Zetterqvist, P; Enell, H; Baccichetti, C; Tenconi, R; Pagon, Ra
Chromosome abnormalities and male infertility. Oligozoospermia: recent progress in andrology
1981-01-01 Tiepolo, Luciano; Zuffardi, Orsetta; Fraccaro, Marco; Giarola, A.
Preferential maternal derivation in inv dup (15): analysis of eight new cases
1981-01-01 Maraschio, Paola; Zuffardi, Orsetta; Bernardi, F; Bozzola, Mauro; De Paoli, C; Fonatsch, C; Ghersini, L; Gimelli, G; Loi, M; Lorini, Renata; Peretti, D; Poloni, L; Tonetti, D; Vanni, R; Zamboni, G.
Agenesis of corpus callosum, ocular and skeletal anomalies (x-linked dominant Aicardi's syndrome)
1982-01-01 Ropers, Hh; Zuffardi, Orsetta; Bianchi, E; Tiepolo, Luciano
Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430 McKusick) is at Xq28, distal to the G6PD locus
1982-01-01 Zuffardi, Orsetta; Fraccaro, Marco
The role of Yp in sex determination: new evidence from X/Y translocations.
1982-01-01 Zuffardi, Orsetta; Maraschio, Paola; LO CURTO, F; Giarola, A; Perotti, L.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Reduced phenotypic effetc of partial trisomy 1q in a X/1 translocation. | 1-gen-1977 | Zuffardi, Orsetta; Tiepolo, Luciano; Scappaticci, S; Francesconi, D; Bianchi, C; Di Natale, B. | |
"Cri du chat" syndrome due to a complex rearrangement of chromosome 5 | 1-gen-1978 | Francesconi, D; Zuffardi, Orsetta; D'Attoma, G; Fraccaro, Marco | |
BSu restriction of DNA from cases exhibiting sex chromosom abnormalities. | 1-gen-1978 | Kinross, J; Fraccaro, Marco; Scappaticci, MARIA ASSUNTA; Tiepolo, Luciano; Zuffardi, Orsetta; Pawlowitzki, Ih; Jones, Kw | |
Chromosome 15 and Prader-Willi syndrome | 1-gen-1978 | Zuffardi, Orsetta; Buhler, Em; Fraccaro, Marco | |
Five unusual karyotypes in Down's syndrome | 1-gen-1979 | Csalone, R; Fraccaro, Marco; Francesconi, D; Pasquali, Francesco; Poloni, L; Zuffardi, Orsetta; Bellomi, A; Crosti, N; Lo Monaco, Gb; Patriarca, Pl; Serventi, M. | |
Familial XX true hermaphroditism and the H-Y antigen. | 1-gen-1979 | Fraccaro, Marco; Tiepolo, Luciano; Zuffardi, Orsetta; Chiumello, G; Di Natale, B; Gargantini, L; Wolf, U. | |
Ring chromosome 12 and latent centromeres | 1-gen-1980 | Zuffardi, Orsetta; Danesino, Cesare; Poloni, L; Pavesi, F; Bianchi, C; Gargantini, L. | |
Trisomy 16q21-->qter | 1-gen-1980 | Garau, A; Crisponi, G; Peretti, D; Vanni, R; Zuffardi, Orsetta | |
Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223. | 1-gen-1980 | Tiepolo, Luciano; Zuffardi, Orsetta; Fraccaro, Marco; Di Natale, B; Gargantini, L; Muller, Cr; Ropers, Hh | |
Turner syndrome patients are H-Y positive. | 1-gen-1980 | Wolf, U; Fraccaro, Marco; Mayerova, A; Hecht, T; Zuffardi, Orsetta | |
Cd bands and centromeric function in dicentric chromosomes | 1-gen-1980 | Maraschio, Paola; Zuffardi, Orsetta; LO CURTO, Francesco | |
A family group with four cases of Kartagener's syndrome | 1-gen-1980 | Zuffardi, Orsetta; Zanon, P; Calligaro, A. | |
Xp deficiencies and female fertility | 1-gen-1980 | Maraschio, Paola; Paquali, F; Zuffardi, Orsetta; Fraccaro, Marco | |
Ribosomal RNA in infertile male carriers of Robertsonian translocations | 1-gen-1980 | Guanti, G; Zuffardi, Orsetta; Tiepolo, Luciano | |
The "cat eye syndrome": dicentric small marker chromosome probably derived from a n. 22 (tetrasomy 22pter-->q11) associated with a characteristic phenotype. | 1-gen-1981 | Schinzel, A; Schmid, W; Fraccaro, Marco; Tiepolo, Luciano; Zuffardi, Orsetta; Opitz, Jm; Lindsten, J; Zetterqvist, P; Enell, H; Baccichetti, C; Tenconi, R; Pagon, Ra | |
Chromosome abnormalities and male infertility. Oligozoospermia: recent progress in andrology | 1-gen-1981 | Tiepolo, Luciano; Zuffardi, Orsetta; Fraccaro, Marco; Giarola, A. | |
Preferential maternal derivation in inv dup (15): analysis of eight new cases | 1-gen-1981 | Maraschio, Paola; Zuffardi, Orsetta; Bernardi, F; Bozzola, Mauro; De Paoli, C; Fonatsch, C; Ghersini, L; Gimelli, G; Loi, M; Lorini, Renata; Peretti, D; Poloni, L; Tonetti, D; Vanni, R; Zamboni, G. | |
Agenesis of corpus callosum, ocular and skeletal anomalies (x-linked dominant Aicardi's syndrome) | 1-gen-1982 | Ropers, Hh; Zuffardi, Orsetta; Bianchi, E; Tiepolo, Luciano | |
Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430 McKusick) is at Xq28, distal to the G6PD locus | 1-gen-1982 | Zuffardi, Orsetta; Fraccaro, Marco | |
The role of Yp in sex determination: new evidence from X/Y translocations. | 1-gen-1982 | Zuffardi, Orsetta; Maraschio, Paola; LO CURTO, F; Giarola, A; Perotti, L. |
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