Sfoglia per Autore
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.
Diagnostic application of first trimester trophobalst sampling in 100 pregnancies
1984-01-01 Simoni, G; Brambati, B; Danesino, Cesare; Terzoli, Gl; Romitti, L; Rossella, F; Fraccaro, Marco
Antenatal sex detrmination
1984-01-01 Simoni, G; Brambati, B; Danesino, Cesare; Fraccaro, Marco
First trimester fetal diagnosis of gentic disorders: clinical evaluation of 250 cases
1985-01-01 Brambati, B; Simoni, G; Danesino, Cesare; Oldrini, A; Ferrazzi, E; Romitti, L; Rossella, F; Ferrari, M; Fraccaro, Marco
Premature centromere disjunction and other chromosome anomalies in Tuberous Sclerosis.
1988-01-01 Fraccaro, Marco; Scappaticci, MARIA ASSUNTA; Cerimele, D; Tondi, M.
Chromosome abnormalities in Tuberous Sclerosis.
1988-01-01 Scappaticci, MARIA ASSUNTA; Cerimele, D; Tondi, M; Vivarelli R., Fois A; Fraccaro, Marco
Shwachman syndrome and chromosome breakage. Letter to the Editor.
1988-01-01 Fraccaro, Marco; Scappaticci, MARIA ASSUNTA; Aricò, M.
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
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
Chromosome abnormalities in Dyskeratosis congenita.
1989-01-01 Scappaticci, MARIA ASSUNTA; Fraccaro, Marco; Cerimele, D.
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
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
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection.
1991-01-01 Maserati, E; Pasquali, Francesco; Zuffardi, Orsetta; Buttitta, P; Cuoco, C; Defant, G; Gimelli, G; Fraccaro, Marco
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.
Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq
1991-01-01 Bardoni, B; Floridia, G; Guioli, S; Peverali, G; Anichini, C; Cisternino, M; Casalone, R; Danesino, Cesare; Fraccaro, Marco; Zuffardi, Orsetta; Camerino, G.
Evidence for an ancestral alphoid domain on the long arm of human chromosome 2
1992-01-01 Avarello, Mr; Pedicini, A; Caiulo, A; Zuffardi, Orsetta; Fraccaro, Marco
Cytogenetics of multiple endocrine neoplasia syndrome. II. Chromosome abnormalities in an insulinoma and a Glaucoma from two subjects with MEN1.
1992-01-01 Scappaticci, MARIA ASSUNTA; Brandi, Ml; Capra, E; Cortinovis, M; Maraschio, Paola; Fraccaro, Marco
Cytogenetic of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasia.
1992-01-01 Scappaticci, MARIA ASSUNTA; Arrigoni, G; Capra, E; Maraschio, Paola; Fraccaro, Marco
Cytogenetic studies in venous tissues from patients with vericose venis.
1994-01-01 Scappaticci, MARIA ASSUNTA; Capra, E; Cortinovis, M; Cortinovis, R; Arbustini, Eloisa; Diegoli, M; Fraccaro, Marco
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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. | |
Diagnostic application of first trimester trophobalst sampling in 100 pregnancies | 1-gen-1984 | Simoni, G; Brambati, B; Danesino, Cesare; Terzoli, Gl; Romitti, L; Rossella, F; Fraccaro, Marco | |
Antenatal sex detrmination | 1-gen-1984 | Simoni, G; Brambati, B; Danesino, Cesare; Fraccaro, Marco | |
First trimester fetal diagnosis of gentic disorders: clinical evaluation of 250 cases | 1-gen-1985 | Brambati, B; Simoni, G; Danesino, Cesare; Oldrini, A; Ferrazzi, E; Romitti, L; Rossella, F; Ferrari, M; Fraccaro, Marco | |
Premature centromere disjunction and other chromosome anomalies in Tuberous Sclerosis. | 1-gen-1988 | Fraccaro, Marco; Scappaticci, MARIA ASSUNTA; Cerimele, D; Tondi, M. | |
Chromosome abnormalities in Tuberous Sclerosis. | 1-gen-1988 | Scappaticci, MARIA ASSUNTA; Cerimele, D; Tondi, M; Vivarelli R., Fois A; Fraccaro, Marco | |
Shwachman syndrome and chromosome breakage. Letter to the Editor. | 1-gen-1988 | Fraccaro, Marco; Scappaticci, MARIA ASSUNTA; Aricò, M. | |
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 | |
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 | |
Chromosome abnormalities in Dyskeratosis congenita. | 1-gen-1989 | Scappaticci, MARIA ASSUNTA; Fraccaro, Marco; Cerimele, D. | |
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 | |
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 | |
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection. | 1-gen-1991 | Maserati, E; Pasquali, Francesco; Zuffardi, Orsetta; Buttitta, P; Cuoco, C; Defant, G; Gimelli, G; Fraccaro, Marco | |
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. | |
Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq | 1-gen-1991 | Bardoni, B; Floridia, G; Guioli, S; Peverali, G; Anichini, C; Cisternino, M; Casalone, R; Danesino, Cesare; Fraccaro, Marco; Zuffardi, Orsetta; Camerino, G. | |
Evidence for an ancestral alphoid domain on the long arm of human chromosome 2 | 1-gen-1992 | Avarello, Mr; Pedicini, A; Caiulo, A; Zuffardi, Orsetta; Fraccaro, Marco | |
Cytogenetics of multiple endocrine neoplasia syndrome. II. Chromosome abnormalities in an insulinoma and a Glaucoma from two subjects with MEN1. | 1-gen-1992 | Scappaticci, MARIA ASSUNTA; Brandi, Ml; Capra, E; Cortinovis, M; Maraschio, Paola; Fraccaro, Marco | |
Cytogenetic of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasia. | 1-gen-1992 | Scappaticci, MARIA ASSUNTA; Arrigoni, G; Capra, E; Maraschio, Paola; Fraccaro, Marco | |
Cytogenetic studies in venous tissues from patients with vericose venis. | 1-gen-1994 | Scappaticci, MARIA ASSUNTA; Capra, E; Cortinovis, M; Cortinovis, R; Arbustini, Eloisa; Diegoli, M; Fraccaro, Marco |
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