Sfoglia per Autore
Identification of a structurally abnormal Y chromosome.
1971-01-01 Scappaticci, MARIA ASSUNTA; Fraccaro, Marco; Tiepolo, Luciano; Turpini, R.
Non fluorescent Y chromosome in a 45,X/46,XY mosaic.
1972-01-01 Scappaticci, MARIA ASSUNTA; LO CURTO, Francesco; Zuffardi, Orsetta; Chierichetti, G; Fraccaro, Marco
Chromosome identification in Chinese hamster pseudodiploid cell line (CHEF-125).
1972-01-01 Scappaticci, MARIA ASSUNTA; LO CURTO, Francesco; Fraccaro, Marco
XO and male phenotype
1974-01-01 Scappaticci, MARIA ASSUNTA; LO CURTO, Francesco; Pucci, E; Scotta, S; Severi, Francesca; Burgio, GIUSEPPE ROBERTO; Fraccaro, Marco
Chromosome identification and karyotypic evolution in a human melanoma cell line (MEL-41).
1974-01-01 Fraccaro, Marco; LO CURTO, Francesco; Scappaticci, MARIA ASSUNTA
15/15 translocation in Prader-Willi syndrome.
1977-01-01 Fraccaro, Marco; Zuffardi, Orsetta; Buhler, E; Jurik, Lp
X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromere.
1977-01-01 Maraschio, Paola; Scappaticci, MARIA ASSUNTA; Ferrari, F; Fraccaro, Marco
"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
The gene for human peptidase A is on band 18q23 and shows triplex and uniplex dosage effect
1978-01-01 Danesino, Cesare; D'Azzo, A; Maraschio, Paola; Fraccaro, Marco
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.
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
Xp deficiencies and female fertility
1980-01-01 Maraschio, Paola; Paquali, F; Zuffardi, Orsetta; Fraccaro, Marco
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.
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
Clonal structural chromosomal rearrangements in primary fibroblastic cultures and in lymphocytes of patients with Werner's syndroe.
1982-01-01 Scappaticci, MARIA ASSUNTA; Cerimele, D; Fraccaro, Marco
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Identification of a structurally abnormal Y chromosome. | 1-gen-1971 | Scappaticci, MARIA ASSUNTA; Fraccaro, Marco; Tiepolo, Luciano; Turpini, R. | |
Non fluorescent Y chromosome in a 45,X/46,XY mosaic. | 1-gen-1972 | Scappaticci, MARIA ASSUNTA; LO CURTO, Francesco; Zuffardi, Orsetta; Chierichetti, G; Fraccaro, Marco | |
Chromosome identification in Chinese hamster pseudodiploid cell line (CHEF-125). | 1-gen-1972 | Scappaticci, MARIA ASSUNTA; LO CURTO, Francesco; Fraccaro, Marco | |
XO and male phenotype | 1-gen-1974 | Scappaticci, MARIA ASSUNTA; LO CURTO, Francesco; Pucci, E; Scotta, S; Severi, Francesca; Burgio, GIUSEPPE ROBERTO; Fraccaro, Marco | |
Chromosome identification and karyotypic evolution in a human melanoma cell line (MEL-41). | 1-gen-1974 | Fraccaro, Marco; LO CURTO, Francesco; Scappaticci, MARIA ASSUNTA | |
15/15 translocation in Prader-Willi syndrome. | 1-gen-1977 | Fraccaro, Marco; Zuffardi, Orsetta; Buhler, E; Jurik, Lp | |
X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromere. | 1-gen-1977 | Maraschio, Paola; Scappaticci, MARIA ASSUNTA; Ferrari, F; Fraccaro, Marco | |
"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 | |
The gene for human peptidase A is on band 18q23 and shows triplex and uniplex dosage effect | 1-gen-1978 | Danesino, Cesare; D'Azzo, A; Maraschio, Paola; Fraccaro, Marco | |
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. | |
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 | |
Xp deficiencies and female fertility | 1-gen-1980 | Maraschio, Paola; Paquali, F; Zuffardi, Orsetta; Fraccaro, Marco | |
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. | |
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 | |
Clonal structural chromosomal rearrangements in primary fibroblastic cultures and in lymphocytes of patients with Werner's syndroe. | 1-gen-1982 | Scappaticci, MARIA ASSUNTA; Cerimele, D; Fraccaro, Marco |
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