Sfoglia per Autore
Cryptic subtelomeric translocation t(2;16)(q37;q24) segregating in a family with unexplained stillbirths and a dysmorphic, slightly retarded child
2001 D. Giardino, P. Finelli, G. Gottardi, D. Clerici, F. Mosca, V. Briscioli, L. Larizza
Refined FISH characterization of a de novo 1p22-p36.2 paracentric inversion and associated 1p21-22 deletion in a patient with signs of 1p36 microdeletion syndrome
2001 P. Finelli, D. Giardino, S. Russo, G. Gottardi, F. Cogliati, G. Grugni, F. Natacci, L. Larizza
Characterization of the t(4;14)(p16.3;q32) in the KMS-18 multiple myeloma cell line
2001 D. Ronchetti, S. Bogni, P. Finelli, L. Lombardi, T. Otsuki, A.T. Maiolo, A. Neri
FISH characterization of t(8;12)(q12;p13) observed as the sole karyotypic anomaly in a myelodysplastic syndrome patient
2001 P. Finelli, N.S. Fracchiolla, D. Giardino, G. Gottardi, D. Lambertenghi Deliliers, A. Cortelezzi, L. Larizza, G. Lambertenghi Deliliers
FISH characterization of a supernumerary r(1)(::cen-->q22::q22-->sq21::) chromosome associated with multiple anomalies and bilateral cataracts
2001 P. Finelli, P. Cavalli, D. Giardino, G. Gottardi, F. Natacci, S. Savasta, L. Larizza
Pure 6p22-pter trisomic patient: refined FISH characterization and genotype-phenotype correlation
2002 D. Giardino, P. Finelli, D. Caufin, G. Gottardi, R. Lo Vasco, L. Turolla, L. Larizza
The High Mobility Group A2 gene is amplified and overexpressed in human prolactinomas
2002 P. Finelli, G. M. Pierantoni, D. Giardino, M. Losa, O. Rodeschini, M. Fedele, E. Valtorta, P. Mortini, C. M. Croce, L. Larizza, A. Fusco
Small familial supernumerary ring chromosome 2: FISH characterization and genotype-phenotype correlation
2002 D. Giardino, P. Finelli, S. Russo, G. Gottardi, O. Rodeschini, M. G. Atza, F. Natacci, L. Larizza
Narrowing the candidate region of Albright hereditary osteodystrophy-like syndrome by deletion mapping in a patient with an unbalanced cryptic translocation t(2;6)(q37.3;q26)
2003 D. Giardino, P. Finelli, G. Gottardi, G. De Canal, M. Della Monica, F. Lonardo, G. Scarano, L. Larizza
The evolutionary history of human chromosome 7
2004 S. Muller, P. Finelli, M. Neusser, J. S. Wienberg
Unbalanced segregation of a complex four-break 5q23-31 insertion in the 5p13 band in a malformed child
2004 D. Giardino, P. Finelli, F. P. Amico, G. Gottardi, R. Civa, G. Corona, G. Nocera, L. Larizza
FISH characterisation of an identical (16)(p11.2p12.2) tandem duplication in two unrelated patients with autistic behaviour
2004 P. Finelli, F. Natacci, M.T. Bonati, G. Gottardi, J.J.M. Engelen, C.E.M. de Die-Smulders, M. Sala, D. Giardino, L. Larizza
High-mobility group A2 gene expression is frequently induced in non-functioning pituitary adenomas (NFPAs), even in the absence of chromosome 12 polysomy
2005 G. M. Pierantoni, P. Finelli, E. Valtorta, D. Giardino, O. Rodeschini, F. Esposito, M. Losa, A. Fusco, L. Larizza
Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories
2005 L. Dalpra, D. Giardino, P. Finelli, C. Corti, C. Valtorta, S. Guerneri, P. Ilardi, R. Fortuna, D. Coviello, G. Nocera, F.P. Amico, E. Martinoli, E. Sala, N. Villa, F. Crosti, F. Chiodo, L.V. Di Cantogno, E. Savin, G. Croci, F. Franchi, G. Venti, E. Donti, V. Migliori, A. Pettinari, S. Bonifacio, C. Centrone, F. Torricelli, S. Rossi, P. Simi, P. Granata, R. Casalone, E. Lenzini, L. Artifoni, V. Pecile, S. Barlati, D. Bellotti, D. Caufin, A. Police, S. Cavani, G. Piombo, M. Pierluigi, L. Larizza
Trisomy 15q25.2-qter in an autistic child: Genotype-phenotype correlations
2005 M.T. Bonati, P. Finelli, D. Giardino, G. Gottardi, W. Roberts, L. Larizza
Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs
2006 D. Giardino, C. Corti, L. Ballarati, P. Finelli, C. Valtorta, G. Botta, M. Giudici, E. Grosso, L. Larizza
Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of 11p15.5 Beckwith-Wiedemann region
2006 S. Russo, P. Finelli, M.P. Recalcati, S. Ferraiuolo, F. Cogliati, B. Dalla Bernardina, M.G. Tibiletti, M. Agosti, M. Sala, M.T. Bonati, L. Larizza
Fetal cell microchimerism in papillary thyroid cancer
2007 V. Cirello, M. Muzza, P. Recalcati, S. Rossi, M. Perrino, P. Finelli, P. Beck Peccoz, L. Fugazzola
13q deletion and CNS anomalies : further insights from karyotype-phenotype analyses of 14 patients
2007 L. Ballarati, E. Rossi, M.T. Bonati, S. Gimelli, P. Maraschio, P. Finelli, S. Giglio, E. Lapi, M.F. Bedeschi, S. Guerneri, G. Arrigo, M.G. Patricelli, T. Mattina, O. Guzzardi, V. Pecile, A. Police, G. Scarano, L. Larizza, O. Zuffardi, D. Giardino
Disruption of Friend of GATA 2 gene (FOG-2) by a de novo t(8;10) chromosomal translocation is associated with heart defects and gonadal dysgenesis
2007 P. Finelli, A. Pincelli, S. Russo, M.T. Bonati, M.P. Recalcati, M. Masciadri, D. Giardino, F. Cavagnini, L. Larizza
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