D. Bettio

发表

Level of HER2/neu amplification in primary tumours and metastases in HER2-positive breast cancer and survival after trastuzumab therapy.

A. Santoro, L. Giordano, G. Gullo, 2013, Breast.

Seizure and EEG Patterns in Angelman's Syndrome

G. Lanzi, F. Lalatta, A. Selicorni, 1995, Journal of child neurology.

Chromosomal abnormalities in miscarriages after different assisted reproduction procedures.

D. Bettio, A. Venci, P. L. Levi Setti, 2008, Placenta.

Administration of temozolomide during and after radiotherapy for newly diagnosed high-grade gliomas excluding glioblastoma multiforme

M. Scorsetti, P. Navarria, A. Santoro, 2007, Journal of Neuro-Oncology.

FISH characterization of small supernumerary marker chromosomes in two Prader-Willi patients.

G. Silvestri, F. Gurrieri, G. Grugni, 1997, American journal of medical genetics.

Analysis and pharmacological modulation of senescence in human epithelial stem cells

S. Ferrari, E. Di Iorio, V. Barbaro, 2022, Journal of cellular and molecular medicine.

Unusual cytogenetic findings in a synovial sarcoma arising in the paranasal sinuses.

P. Gaetani, P. Bianchi, P. Colombo, 2004, Cancer genetics and cytogenetics.

Near-tetraploid karyotype with an isochromosome 17q as the sole structural chromosomal rearrangement in a case of testicular granulocytic sarcoma.

B. Sarina, D. Bettio, A. Venci, 2008, Cancer genetics and cytogenetics.

Cytogenetic study of pituitary adenomas.

M. Losa, L. Persani, D. Giardino, 1997, Cancer genetics and cytogenetics.

FISH analysis in Prader-Willi and Angelman syndrome patients.

A. Selicorni, G. Grugni, D. Giardino, 1995, American journal of medical genetics.

Clinical and molecular cytogenetic studies in three infertile patients with mosaic rearranged Y chromosomes.

D. Bettio, P. Setti, A. Venci, 2006, Human reproduction.

Prenatal diagnosis of del(9)(p24): a sex reverse case

S. Stioui, G. Giordano, D. Bettio, 2005, Prenatal diagnosis.

Cytogenetic abnormalities detected by direct analysis in a case of choriocarcinoma.

D. Giardino, G. Simoni, D. Bettio, 1993, Cancer genetics and cytogenetics.

Level of HER2/neu gene amplification as a predictive factor of response to trastuzumab-based therapy in patients with HER2-positive metastatic breast cancer

V. Torri, A. Santoro, G. Gullo, 2009, Investigational New Drugs.

FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes.

D. Giardino, L. Larizza, G. Gottardi, 1999, American journal of medical genetics.

A de novo 6q11—q15 duplication investigated by chromosome painting

D. Giardino, V. Briscioli, D. Bettio, 1994, Clinical genetics.

Prevalence and distribution of chromosome abnormalities in a sample of first trimester internal abortions.

B. Brambati, M. Fraccaro, G. Simoni, 1987, Human reproduction.

Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenoma.

D. Giardino, L. Larizza, P. Riva, 1996, Acta geneticae medicae et gemellologiae.

Seven cases of trisomy 3 mosaicism in chorionic villi

G. Simoni, S. Guerneri, D. Bettio, 1989, Prenatal diagnosis.

Trisomy 18 mosaicism in a woman with normal intelligence

P. Bianchi, D. Bettio, P. Setti, 2003, American journal of medical genetics. Part A.

The displacement of frataxin from the mitochondrial cristae correlates with abnormal respiratory supercomplexes formation and bioenergetic defects in cells of Friedreich ataxia patients

M. Soriano, L. Salviati, I. Szabó, 2021, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Familial translocation (X;3) (p22.3;p23): chromosomal in situ suppression (CISS) hybridization and inactivation pattern study

D. Giardino, D. Bettio, N. Rizzi, 1994, Clinical genetics.

A fluorescence in situ hybridization (FISH) procedure to assist in differentiating benign from malignant melanocytic lesions.

M. Mihm, A. Piris, L. Scopsi, 2009, Pathologica.

Molecular cytogenetic and clinical findings in a patient with a small supernumerary r(8) mosaicism

D. Ledbetter, A. Vignoli, R. Carrozzo, 2008, American journal of medical genetics. Part A.

Tetrasomy 5p mosaicism due to an additional isochromosome 5p in a man with normal phenotype

D. Bettio, A. Venci, 2009, American journal of medical genetics. Part A.

Case of paracentric inversion 19p.

D. Giardino, D. Bettio, N. Rizzi, 1995, American journal of medical genetics.

Lung cancer in which the hypothesis of multi-step progression is confirmed by array-CGH results: A case report

M. Alloisio, A. Santoro, D. Bettio, 2015, Experimental and therapeutic medicine.

Cytogenetic findings in lung cancer that illuminate its biological history from adenomatous hyperplasia to bronchioalveolar carcinoma to adenocarcinoma: A case report

M. Alloisio, P. Spaggiari, U. Cariboni, 2012, Experimental and therapeutic medicine.

45,X product of conception after preimplantation genetic diagnosis and euploid embryo transfer: evidence of a spontaneous conception confirmed by DNA fingerprinting

L. Rienzi, A. Capalbo, F. Ubaldi, 2016, Reproductive Biology and Endocrinology.

Acute promyelocytic leukemia with a cryptic insertion of RARA into PML on chromosome 15 due to uniparental isodisomy: A case report

O. Spinelli, D. Bettio, A. Venci, 2017, Oncology letters.

Orphenadrine Serum Levels in a Poisoned Patient

M. Furlanut, P. Benetello, D. Bettio, 1985, Human toxicology.

Clinical and molecular cytogenetic studies in three infertile patients with mosaic rearranged Y chromosomes.

D. Bettio, P. Setti, A. Venci, 2006, Human reproduction.

Fluorescent in situ hybridization (FISH) in the differential diagnosis of ground-glass opacities in the lung.

U. Cariboni, D. Bettio, M. Infante, 2011, Lung cancer.