SCAPPATICCI, MARIA ASSUNTA

SCAPPATICCI, MARIA ASSUNTA  

DIPARTIMENTO DI MEDICINA MOLECOLARE  

Mostra records
Risultati 1 - 20 di 51 (tempo di esecuzione: 0.033 secondi).
Titolo Data di pubblicazione Autore(i) File
"Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosis. 1-gen-1976 Gimelli, G; Porro, E; Santi, F; Scappaticci, MARIA ASSUNTA; Zuffardi, Orsetta
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 family with Autosomal Dominant leukodystrophy linked to 5q23.2-q23.3. 1-gen-2009 Brussino, A; Vaula, G; Cagnoli, C; Panza, E; Seri, M; Di Gregorio, E; Scappaticci, MARIA ASSUNTA; Camanini, Silvia; Daniele, D; Bradac, Gb; Pinessi, L; Cavalieri, S; Grosso, E; Migone, N; Brusco, A.
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.
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
Can GH induce chromosome breaks or microsatellite instability in GH-deficient children? 1-gen-2004 Olivieri, Carla; Danesino, Cesare; Scappaticci, MARIA ASSUNTA; Bozzola, Mauro
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 abnormalities in a case of pituitary adenoma. 1-gen-1993 Capra, E; Rindi, Guido; Santi, G; Spina, Mp; Scappaticci, MARIA ASSUNTA
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
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.
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.
Citochimica, autoradiografia e ultrastruttura di cellule della granulosa ovarica umana "in vitro". 1-gen-1975 Magrini, Umberto; Scappaticci, MARIA ASSUNTA; Tiepolo, Luciano; Danesino, Cesare
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
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