TESTA, BARBARA
TESTA, BARBARA
Dipartimento di Biologia
Breast cancer in West Africa: molecular analysis of BRCA genes in early-onset breast cancer patients in Burkina Faso
2021-01-01 Biancolella, M; Ouedraogo, Nlm; Zongo, N; Zohoncon, Tm; Testa, B; Rizzacasa, B; Latini, A; Conte, C; Compaore, Tr; Ouedraogo, CMR-; Traore, Ss; Simpore, J; Novelli, G
Coexistence of Two Novel Mutations in CDKN2A and PMS1 Genes in a Single Patient Identifies a New and Severe Cancer Predisposition Syndrome
2017-05-04 Cassone, M; Baghernajad Salehi, L; Biancolella, M; Testa, B; Mastrogiorgio, G; Lanciotti, S; Rosaria D'Apice3, M; Novelli, G; Sangiuolo, Fc; Tedaldi2, G; Tebaldi, M
Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants
2023-07-01 Siracusano, M; Riccioni, A; Frattale, I; Arturi, L; Dante, C; Galasso, C; Gialloreti, Le; Conteduca, G; Testa, B; Malacarne, M; Coviello, D; Mazzone, L
Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: A novel recognizable microdeletion syndrome?
2015-01-01 D'Apice, Mr; Novelli, A; di Masi, A; Biancolella, M; Antoccia, A; Gullotta, F; Licata, N; Minella, D; Testa, B; Nardone, A; Palmieri, G; Calabrese, E; Biancone, L; Tanzarella, C; Frontali, M; Sangiuolo, Fc; Novelli, G; Pallone, F
Genetics and genomics of breast cancer: update and translational perspectives
2021-01-01 Biancolella, M; Testa, B; Baghernajad Salehi, L; D'Apice, Mr; Novelli, G
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2021 | Breast cancer in West Africa: molecular analysis of BRCA genes in early-onset breast cancer patients in Burkina Faso | Biancolella, M; Ouedraogo, Nlm; Zongo, N; Zohoncon, Tm; Testa, B; Rizzacasa, B; Latini, A; Conte, C; Compaore, Tr; Ouedraogo, CMR-; Traore, Ss; Simpore, J; Novelli, G | Articolo su rivista | |
| 4-mag-2017 | Coexistence of Two Novel Mutations in CDKN2A and PMS1 Genes in a Single Patient Identifies a New and Severe Cancer Predisposition Syndrome | Cassone, M; Baghernajad Salehi, L; Biancolella, M; Testa, B; Mastrogiorgio, G; Lanciotti, S; Rosaria D'Apice3, M; Novelli, G; Sangiuolo, Fc; Tedaldi2, G; Tebaldi, M | Articolo su rivista | |
| 1-lug-2023 | Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants | Siracusano, M; Riccioni, A; Frattale, I; Arturi, L; Dante, C; Galasso, C; Gialloreti, Le; Conteduca, G; Testa, B; Malacarne, M; Coviello, D; Mazzone, L | Articolo su rivista | |
| 1-gen-2015 | Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: A novel recognizable microdeletion syndrome? | D'Apice, Mr; Novelli, A; di Masi, A; Biancolella, M; Antoccia, A; Gullotta, F; Licata, N; Minella, D; Testa, B; Nardone, A; Palmieri, G; Calabrese, E; Biancone, L; Tanzarella, C; Frontali, M; Sangiuolo, Fc; Novelli, G; Pallone, F | Articolo su rivista | |
| 1-gen-2021 | Genetics and genomics of breast cancer: update and translational perspectives | Biancolella, M; Testa, B; Baghernajad Salehi, L; D'Apice, Mr; Novelli, G | Articolo su rivista |