Sfoglia per Autore
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
Multiple clonal chromosome abnormalities in a superficial basal cell epithelioma.
1989-01-01 Scappaticci, MARIA ASSUNTA; Fraccaro, M; Orecchia, Giovanni
Chromosome abnormalities in Dyskeratosis congenita.
1989-01-01 Scappaticci, MARIA ASSUNTA; Fraccaro, Marco; Cerimele, D.
Chromosome instability in lymphocytes from a patient with Werner's syndrome is not associated with DNA repair defect.
1989-01-01 Stefanini, M; Scappaticci, MARIA ASSUNTA; Lagomarsini, P; Borroni, Giovanni; Berardesca, E; Nuzzo, F.
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
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
Chromosome abnormalities in a case of pituitary adenoma.
1993-01-01 Capra, E; Rindi, Guido; Santi, G; Spina, Mp; Scappaticci, MARIA ASSUNTA
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
homozygosity mapping of the Werner syndrome locus (WRN).
1994-01-01 Nakura, J; Wijsma, Em; Miki, T; Kamino, K; Yu, Ce; Oshima, J; Fukuchi, Ki; Piussan, C; Melaragno, Mi; Epstein, Cj; Scappaticci, MARIA ASSUNTA; Fraccaro, Marco; Matsumura, T; Murano, S; Yoshida, S; Fujiwara, Y; Saida, T; Ogihara, T; Martin, Gm; Schellenberg, Gd
Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulp.
1994-01-01 Casasco, Andrea; Maserati, E; Giordano, M; Casasco, M; Ciuffreda, M; Sander, S; Danova, M; Scappaticci, MARIA ASSUNTA; Calligaro, Alberto; Springall, Dr; Polak, J. M.
A search for double minute chromosomes in cultured lymphocytes from different types of tumors.
1995-01-01 Scappaticci, MARIA ASSUNTA; Fossati, Gs; Valenti, L; Scabini, M; Tateo, S; Nastasi, G; Spina, Mp; Capra, E.
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosomes 18p11.1-21.1 markers.
1996-01-01 Goddard, Kab; Fraccaro, Marco; Scappaticci, MARIA ASSUNTA
Focal dermal hypoplasia: report of a family with 7 affected women in 3 generations.
1996-01-01 Bellosta, M; Trespiolli, D; Ghiselli, E; Capra, E; Scappaticci, MARIA ASSUNTA
Lipoid proteinosis: lipid inclusions in fibroblasts.
1996-01-01 Capra, E; Scappaticci, MARIA ASSUNTA; Cottoni, F.
Concurrent cytogenetic and molecular investigations in uterine and ovarian neoplasms
1998-01-01 Minelli, Antonella; Capra, E.; Dellavecchia, C.; Danesino, Cesare; Olivieri, Carla; Tateo, S.; Tenti, P.; Scappaticci, MARIA ASSUNTA
Chromosomal breaks in lymphocytes from respiratory syncytial virus-infected infants.
1999-01-01 Bozzola, Mauro; Marchi, Antonietta; Severi, Francesca; Comoli, Patrizia; Capra, E; Percivalle, E; Scappaticci, MARIA ASSUNTA
Chromosome instability in cultured lymphocytes of patients with ovarian or uterine cancer.
1999-01-01 Scappaticci, MARIA ASSUNTA; Pasquali, Francesco; Capra, E; Olivieri, Carla; Tateo, S.
Isochromosome (7)(q10) in Shwachman Syndrome Without MDS/AML and Role of Chromosome 7 Anomalies in Myeloproliferative Disorders
2000-01-01 Maserati, E.; Minelli, Antonella; Olivieri, Carla; Bonvini, L.; Marchi, Antonietta; Bozzola, Mauro; Danesino, Cesare; Scappaticci, MARIA ASSUNTA; Pasquali, F.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 | |
Multiple clonal chromosome abnormalities in a superficial basal cell epithelioma. | 1-gen-1989 | Scappaticci, MARIA ASSUNTA; Fraccaro, M; Orecchia, Giovanni | |
Chromosome abnormalities in Dyskeratosis congenita. | 1-gen-1989 | Scappaticci, MARIA ASSUNTA; Fraccaro, Marco; Cerimele, D. | |
Chromosome instability in lymphocytes from a patient with Werner's syndrome is not associated with DNA repair defect. | 1-gen-1989 | Stefanini, M; Scappaticci, MARIA ASSUNTA; Lagomarsini, P; Borroni, Giovanni; Berardesca, E; Nuzzo, F. | |
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 | |
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 | |
Chromosome abnormalities in a case of pituitary adenoma. | 1-gen-1993 | Capra, E; Rindi, Guido; Santi, G; Spina, Mp; Scappaticci, MARIA ASSUNTA | |
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 | |
homozygosity mapping of the Werner syndrome locus (WRN). | 1-gen-1994 | Nakura, J; Wijsma, Em; Miki, T; Kamino, K; Yu, Ce; Oshima, J; Fukuchi, Ki; Piussan, C; Melaragno, Mi; Epstein, Cj; Scappaticci, MARIA ASSUNTA; Fraccaro, Marco; Matsumura, T; Murano, S; Yoshida, S; Fujiwara, Y; Saida, T; Ogihara, T; Martin, Gm; Schellenberg, Gd | |
Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulp. | 1-gen-1994 | Casasco, Andrea; Maserati, E; Giordano, M; Casasco, M; Ciuffreda, M; Sander, S; Danova, M; Scappaticci, MARIA ASSUNTA; Calligaro, Alberto; Springall, Dr; Polak, J. M. | |
A search for double minute chromosomes in cultured lymphocytes from different types of tumors. | 1-gen-1995 | Scappaticci, MARIA ASSUNTA; Fossati, Gs; Valenti, L; Scabini, M; Tateo, S; Nastasi, G; Spina, Mp; Capra, E. | |
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosomes 18p11.1-21.1 markers. | 1-gen-1996 | Goddard, Kab; Fraccaro, Marco; Scappaticci, MARIA ASSUNTA | |
Focal dermal hypoplasia: report of a family with 7 affected women in 3 generations. | 1-gen-1996 | Bellosta, M; Trespiolli, D; Ghiselli, E; Capra, E; Scappaticci, MARIA ASSUNTA | |
Lipoid proteinosis: lipid inclusions in fibroblasts. | 1-gen-1996 | Capra, E; Scappaticci, MARIA ASSUNTA; Cottoni, F. | |
Concurrent cytogenetic and molecular investigations in uterine and ovarian neoplasms | 1-gen-1998 | Minelli, Antonella; Capra, E.; Dellavecchia, C.; Danesino, Cesare; Olivieri, Carla; Tateo, S.; Tenti, P.; Scappaticci, MARIA ASSUNTA | |
Chromosomal breaks in lymphocytes from respiratory syncytial virus-infected infants. | 1-gen-1999 | Bozzola, Mauro; Marchi, Antonietta; Severi, Francesca; Comoli, Patrizia; Capra, E; Percivalle, E; Scappaticci, MARIA ASSUNTA | |
Chromosome instability in cultured lymphocytes of patients with ovarian or uterine cancer. | 1-gen-1999 | Scappaticci, MARIA ASSUNTA; Pasquali, Francesco; Capra, E; Olivieri, Carla; Tateo, S. | |
Isochromosome (7)(q10) in Shwachman Syndrome Without MDS/AML and Role of Chromosome 7 Anomalies in Myeloproliferative Disorders | 1-gen-2000 | Maserati, E.; Minelli, Antonella; Olivieri, Carla; Bonvini, L.; Marchi, Antonietta; Bozzola, Mauro; Danesino, Cesare; Scappaticci, MARIA ASSUNTA; Pasquali, F. |
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