Sfoglia per Autore
Olfactory receptor genes and chromosome 11 structural aberrations: Players or spectators?
2024 Redaelli, S; Grati, F; Tritto, V; Giannuzzi, G; Recalcati, M; Sala, E; Villa, N; Crosti, F; Roversi, G; Malvestiti, F; Zanatta, V; Repetti, E; Rodeschini, O; Valtorta, C; Catusi, I; Romitti, L; Martinoli, E; Conconi, D; Dalprà, L; Lavitrano, M; Riva, P; Bentivegna, A
A DNA damage response-like phenotype defines a third of colon cancers at onset
2023 Mauro, S; Bolognesi, M; Villa, N; Capitoli, G; Furia, L; Mascadri, F; Zucchini, N; Totis, M; Faretta, M; Galimberti, S; Bovo, G; Cattoretti, G
Characterization of Chromosomal Breakpoints in 12 Cases with 8p Rearrangements Defines a Continuum of Fragility of the Region
2022 Redaelli, S; Conconi, D; Sala, E; Villa, N; Crosti, F; Roversi, G; Catusi, I; Valtorta, C; Recalcati, M; Dalpra, L; Lavitrano, M; Bentivegna, A
Human chromosome 18 and acrocentrics: A dangerous liaison
2021 Villa, N; Redaelli, S; Sala, E; Conconi, D; Romitti, L; Manfredini, E; Crosti, F; Roversi, G; Lavitrano, M; Rodeschini, O; Recalcati, M; Piazza, R; Dalpra, L; Riva, P; Bentivegna, A
Instability of short arm of acrocentric chromosomes: Lesson from non-acrocentric satellited chromosomes. report of 24 unrelated cases
2020 Redaelli, S; Conconi, D; Villa, N; Sala, E; Crosti, F; Corti, C; Catusi, I; Garzo, M; Romitti, L; Martinoli, E; Patrizi, A; Malgara, R; Recalcati, M; Dalpra, L; Lavitrano, M; Riva, P; Roversi, G; Bentivegna, A
Refining the Phenotype of Recurrent Rearrangements of Chromosome 16
2019 Redaelli, S; Maitz, S; Crosti, F; Sala, E; Villa, N; Spaccini, L; Selicorni, A; Rigoldi, M; Conconi, D; Dalprà, L; Roversi, G; Bentivegna, A
Interphase FISH: A Helpful Assay in Prenatal Cytogenetics Diagnosis
2019 Sala, E; Conconi, D; Crosti, F; Villa, N; Redaelli, S; Roversi, G
Familiar unbalanced complex rearrangements involving 13 p-arm: Description of two cases
2018 Conconi, D; Villa, N; Redaelli, S; Sala, E; Crosti, F; Maitz, S; Rigoldi, M; Parini, R; Dalprà, L; Lavitrano, M; Roversi, G
A new case report of severe mucopolysaccharidosis type VII: Diagnosis, treatment with haematopoietic cell transplantation and prenatal diagnosis in a second pregnancy 11 Medical and Health Sciences 1114 Paediatrics and Reproductive Medicine
2018 Furlan, F; Rovelli, A; Rigoldi, M; Filocamo, M; Tappino, B; Friday, D; Gasperini, S; Mariani, S; Izzi, C; Bondioni, M; Gellera, C; Venerando, A; Villa, N; Del Carmen Rodriguez Perez, M; Pavan, F; Biondi, A; Parini, R
19q12q13.2 duplication syndrome: Neuropsychiatric long-term follow-up of a new case and literature update
2017 Nacinovich, R; Villa, N; Broggi, F; Tavaniello, C; Bomba, M; Conconi, D; Redaelli, S; Sala, E; Lavitrano, M; Neri, F
A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning
2017 Villa, N; Conconi, D; Gambel Benussi, D; Tornese, G; Crosti, F; Sala, E; Dalpra', L; Pecile, V
14q32.3-qter trisomic segment: A case report and literature review
2016 Villa, N; Scatigno, A; Redaelli, S; Conconi, D; Cianci, P; Farina, C; Fossati, C; Dalpra', L; Maitz, S; Selicorni, A
Hodgkin lymphoma in a patient with mosaic trisomy 18: First clinical observation
2016 Motta, S; Sala, D; Sala, A; Cazzaniga, G; Giudici, G; Villa, N; Biondi, A; Selicorni, A
Interstitial 11q deletion: genomic characterization and neuropsychiatric follow up from early infancy to adolescence and literature review
2014 Nacinovich, R; Villa, N; Redaelli, S; Broggi, F; Bomba, M; Stoppa, P; Scatigno, A; Selicorni, A; Dalprà, L; Neri, F
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