Sfoglia per Autore
Fetal cell microchimerism in papillary thyroid cancer
2007 V. Cirello, M. Muzza, M.P. Recalcati, S. Rossi, M. Perrino, P. Finelli, P. Beck-Peccoz, L. Fugazzola
Fetal cell microchimerism in papillary thyroid cancer : a possibile role in tumor demage and tissue repair
2008 V. Cirello, M.P. Recalcati, M. Muzza, S. Rossi, M. Perrino, P. Beck-Peccoz, P. Finelli, L. Fugazzola
Misbehaviour of XIST RNA in breast cancer cells
2008 S.M. Tabano, L. Monti, M. Recalcati, M. Gariboldi, F.R. Grati, P. Finelli, P. Radice, M. Miozzo, S.M. Sirchia
Identification of balanced 4p16 paracentric inversions in three patients with Wolf-Hirschhorn phenotype not deleted for the WHS critical region
2011 P. Finelli, M. Crippa, E. Valtorta, C. Castronovo, M. Masciadri, S. Russo, M. Recalcati, D. Rusconi, D. Giardino, M. Bonati, F. Natacci, P. Castelluccio, L. Larizza
Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype
2012 P. Finelli, S. Sirchia, M. Masciadri, M. Crippa, M. Recalcati, D. Rusconi, D. Giardino, L. Monti, F. Cogliati, F. Faravelli, F. Natacci, L. Zoccante, B. Bernardina, S. Russo, L. Larizza
Complex rearrangement involving 9p deletion and duplication in a syndromic patient : Genotype/phenotype correlation and review of the literature
2012 M.P. Recalcati, M. Bellini, L. Norsa, L. Ballarati, R. Caselli, S. Russo, L. Larizza, D. Giardino
Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome
2014 C. Castronovo, R. Rossetti, D. Rusconi, M.P. Recalcati, C. Cacciatore, E. Beccaria, V. Calcaterra, P. Invernizzi, D. Larizza, P. Finelli, L. Persani
7p22.1 microduplication syndrome : clinical and molecular characterization of an adult case and review of the literature
2015 R. Caselli, L. Ballarati, A. Vignoli, A. Peron, M.P. Recalcati, I. Catusi, L. Larizza, D. Giardino
Instability of short arm of acrocentric chromosomes : Lesson from non-acrocentric satellited chromosomes. Report of 24 unrelated cases
2020 S. Redaelli, D. Conconi, N. Villa, E. Sala, F. Crosti, C. Corti, I. Catusi, M. Garzo, L. Romitti, E. Martinoli, A. Patrizi, R. Malgara, M.P. Recalcati, L. Dalprà, M. Lavitrano, P. Riva, G. Roversi, A. Bentivegna
Ring Chromosome 20 Syndrome : Genetics, Clinical Characteristics, and Overlapping Phenotypes
2020 A. Peron, I. Catusi, M.P. Recalcati, L. Calzari, L. Larizza, A. Vignoli, M.P. Canevini
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