FRACCARO, MARCO
FRACCARO, MARCO
DIPARTIMENTO DI PATOLOGIA UMANA ED EREDITARIA (attivo dal 01/01/1900 al 28/02/2011)
"Cri du chat" syndrome due to a complex rearrangement of chromosome 5
1978-01-01 Francesconi, D; Zuffardi, Orsetta; D'Attoma, G; Fraccaro, Marco
15/15 translocation in Prader-Willi syndrome.
1977-01-01 Fraccaro, Marco; Zuffardi, Orsetta; Buhler, E; Jurik, Lp
A clonal t(),12)(q32q21) in cultured fibroblasts from a case of Bowen's disease.
1989-01-01 Scappaticci, MARIA ASSUNTA; Lambaise, S; Fraccaro, Marco; Orecchia, Giovanni
A clonal t(9;12)(q32;q21) in cultured fibroblasts from a case of Bowen's disease
1989-01-01 Scappaticci, MARIA ASSUNTA; Lambiase, Simonetta; Fraccaro, Marco; Orecchia, Giovanni
A deletion of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis
1991-01-01 Bardoni, B; Zuffardi, Orsetta; Guioli, S; Ballabio, A; Simi, P; Cavalli, P; Grimoldi, Mg; Fraccaro, Marco; Camerino, G.
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal
1994-01-01 Bardoni, B; Zanaria, E; Floridia, G; Worley, Kc; Toini, G; Ferrante, E; Chiumello, G; Mccabe, Erb; Fraccaro, Marco; Zuffardi, Orsetta; Camerino, G.
A novel mechnaism for the origin of supernumerary marker chromosomes
1996-01-01 Maraschio, Paola; Tupler, R; Rossi, Elena; Barbierato, L; Uccellatore, F; Rocchi, M; Zuffardi, Orsetta; Fraccaro, Marco
Antenatal sex detrmination
1984-01-01 Simoni, G; Brambati, B; Danesino, Cesare; Fraccaro, Marco
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
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
Chromosome abnormalities and male infertility. Oligozoospermia: recent progress in andrology
1981-01-01 Tiepolo, Luciano; Zuffardi, Orsetta; Fraccaro, Marco; Giarola, A.
Chromosome abnormalities in Dyskeratosis congenita.
1989-01-01 Scappaticci, MARIA ASSUNTA; Fraccaro, Marco; Cerimele, D.
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1.
1991-01-01 Scappaticci, MARIA ASSUNTA; Maraschio, Paola; del Ciotto, N; Fossati, Gs; Zonta, Aris; Fraccaro, Marco
Chromosome abnormalities in Tuberous Sclerosis.
1988-01-01 Scappaticci, MARIA ASSUNTA; Cerimele, D; Tondi, M; Vivarelli R., Fois A; 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
Chromosome identification in Chinese hamster pseudodiploid cell line (CHEF-125).
1972-01-01 Scappaticci, MARIA ASSUNTA; LO CURTO, Francesco; Fraccaro, Marco
Clonal chromosome abnormalities with preferential ilvolvement of chromosome 3 in patient with Porokeratosi of Mibelli.
1989-01-01 Scappaticci, MARIA ASSUNTA; Lambiase, Simonetta; Orecchia, Giovanni; 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
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
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
"Cri du chat" syndrome due to a complex rearrangement of chromosome 5 | 1-gen-1978 | Francesconi, D; Zuffardi, Orsetta; D'Attoma, G; Fraccaro, Marco | |
15/15 translocation in Prader-Willi syndrome. | 1-gen-1977 | Fraccaro, Marco; Zuffardi, Orsetta; Buhler, E; Jurik, Lp | |
A clonal t(),12)(q32q21) in cultured fibroblasts from a case of Bowen's disease. | 1-gen-1989 | Scappaticci, MARIA ASSUNTA; Lambaise, S; Fraccaro, Marco; Orecchia, Giovanni | |
A clonal t(9;12)(q32;q21) in cultured fibroblasts from a case of Bowen's disease | 1-gen-1989 | Scappaticci, MARIA ASSUNTA; Lambiase, Simonetta; Fraccaro, Marco; Orecchia, Giovanni | |
A deletion of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis | 1-gen-1991 | Bardoni, B; Zuffardi, Orsetta; Guioli, S; Ballabio, A; Simi, P; Cavalli, P; Grimoldi, Mg; Fraccaro, Marco; Camerino, G. | |
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal | 1-gen-1994 | Bardoni, B; Zanaria, E; Floridia, G; Worley, Kc; Toini, G; Ferrante, E; Chiumello, G; Mccabe, Erb; Fraccaro, Marco; Zuffardi, Orsetta; Camerino, G. | |
A novel mechnaism for the origin of supernumerary marker chromosomes | 1-gen-1996 | Maraschio, Paola; Tupler, R; Rossi, Elena; Barbierato, L; Uccellatore, F; Rocchi, M; Zuffardi, Orsetta; Fraccaro, Marco | |
Antenatal sex detrmination | 1-gen-1984 | Simoni, G; Brambati, B; Danesino, Cesare; Fraccaro, Marco | |
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 | |
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 | |
Chromosome abnormalities and male infertility. Oligozoospermia: recent progress in andrology | 1-gen-1981 | Tiepolo, Luciano; Zuffardi, Orsetta; Fraccaro, Marco; Giarola, A. | |
Chromosome abnormalities in Dyskeratosis congenita. | 1-gen-1989 | Scappaticci, MARIA ASSUNTA; Fraccaro, Marco; Cerimele, D. | |
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1. | 1-gen-1991 | Scappaticci, MARIA ASSUNTA; Maraschio, Paola; del Ciotto, N; Fossati, Gs; Zonta, Aris; Fraccaro, Marco | |
Chromosome abnormalities in Tuberous Sclerosis. | 1-gen-1988 | Scappaticci, MARIA ASSUNTA; Cerimele, D; Tondi, M; Vivarelli R., Fois A; 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 | |
Chromosome identification in Chinese hamster pseudodiploid cell line (CHEF-125). | 1-gen-1972 | Scappaticci, MARIA ASSUNTA; LO CURTO, Francesco; Fraccaro, Marco | |
Clonal chromosome abnormalities with preferential ilvolvement of chromosome 3 in patient with Porokeratosi of Mibelli. | 1-gen-1989 | Scappaticci, MARIA ASSUNTA; Lambiase, Simonetta; Orecchia, Giovanni; 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 | |
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 |