检索结果 - Costanza, Jole
- Showing 1 - 13 results of 13
-
1
-
2
-
3
-
4
-
5
A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability: a case report 由 Moresco, Giada, Costanza, Jole, Santaniello, Carlo, Rondinone, Ornella, Grilli, Federico, Prada, Elisabetta, Orcesi, Simona, Coro, Ilaria, Pichiecchio, Anna, Marchisio, Paola, Miozzo, Monica, Fontana, Laura, Milani, Donatella
出版 2021Text -
6
PTEN Expression as a Complementary Biomarker for Mismatch Repair Testing in Breast Cancer 由 Lopez, Gianluca, Noale, Marianna, Corti, Chiara, Gaudioso, Gabriella, Sajjadi, Elham, Venetis, Konstantinos, Gambini, Donatella, Runza, Letterio, Costanza, Jole, Pesenti, Chiara, Grossi, Francesco, Maggi, Stefania, Ferrero, Stefano, Bosari, Silvano, Fusco, Nicola
出版 2020Text -
7
The Genetic Landscape of Human Glioblastoma and Matched Primary Cancer Stem Cells Reveals Intratumour Similarity and Intertumour Heterogeneity 由 Pesenti, Chiara, Navone, Stefania Elena, Guarnaccia, Laura, Terrasi, Andrea, Costanza, Jole, Silipigni, Rosamaria, Guarneri, Silvana, Fusco, Nicola, Fontana, Laura, Locatelli, Marco, Rampini, Paolo, Campanella, Rolando, Tabano, Silvia, Miozzo, Monica, Marfia, Giovanni
出版 2019Text -
8
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 由 Fontana, Laura, Bedeschi, Maria F., Cagnoli, Giulia A., Costanza, Jole, Persico, Nicola, Gangi, Silvana, Porro, Matteo, Ajmone, Paola F., Colapietro, Patrizia, Santaniello, Carlo, Crippa, Milena, Sirchia, Silvia M., Miozzo, Monica, Tabano, Silvia
出版 2020Text -
9
A HS6ST2 gene variant associated with X‐linked intellectual disability and severe myopia in two male twins 由 Paganini, Leda, Hadi, Loubna A., Chetta, Massimiliano, Rovina, Davide, Fontana, Laura, Colapietro, Patrizia, Bonaparte, Eleonora, Pezzani, Lidia, Marchisio, Paola, Tabano, Silvia M., Costanza, Jole, Sirchia, Silvia M., Riboni, Laura, Milani, Donatella, Miozzo, Monica
出版 2018Text -
10
Extensive Placental Methylation Profiling in Normal Pregnancies 由 Rondinone, Ornella, Murgia, Alessio, Costanza, Jole, Tabano, Silvia, Camanni, Margherita, Corsaro, Luigi, Fontana, Laura, Colapietro, Patrizia, Calzari, Luciano, Motta, Silvia, Santaniello, Carlo, Radaelli, Tatjana, Ferrazzi, Enrico, Bosari, Silvano, Gentilini, Davide, Sirchia, Silvia Maria, Miozzo, Monica
出版 2021Text -
11
Correction: Rondinone et al. Extensive Placental Methylation Profiling in Normal Pregnancies. Int. J. Mol. Sci. 2021, 22, 2136 由 Rondinone, Ornella, Murgia, Alessio, Costanza, Jole, Tabano, Silvia, Camanni, Margherita, Corsaro, Luigi, Fontana, Laura, Colapietro, Patrizia, Calzari, Luciano, Motta, Silvia, Santaniello, Carlo, Radaelli, Tatjana, Ferrazzi, Enrico, Bosari, Silvano, Gentilini, Davide, Sirchia, Silvia Maria, Miozzo, Monica
出版 2022Text -
12
Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic Brachydactyly 由 Elli, Francesca Marta, Mattinzoli, Deborah, Lucca, Camilla, Piu, Matteo, Maffini, Maria A., Costanza, Jole, Fontana, Laura, Santaniello, Carlo, Forino, Concetta, Milani, Donatella, Bonati, Maria Teresa, Secco, Andrea, Gastaldi, Roberto, Alfieri, Carlo, Messa, Piergiorgio, Miozzo, Monica, Arosio, Maura, Mantovani, Giovanna
出版 2022Text -
13
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 由 Costanza, Jole, Camanni, Margherita, Ferrari, Maria Maddalena, De Cosmi, Valentina, Tabano, Silvia, Fontana, Laura, Radaelli, Tatjana, Privitera, Giulia, Alberico, Daniela, Colapietro, Patrizia, Motta, Silvia, Sirchia, Silvia, Stampalija, Tamara, Tabasso, Chiara, Roggero, Paola, Parazzini, Fabio, Mosca, Fabio, Ferrazzi, Enrico, Bosari, Silvano, Miozzo, Monica, Agostoni, Carlo
出版 2021Text