Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Monia Rinaldini"'
Autor:
Giuseppina Comitini, Veronica Barbieri, Paola Bonasoni, Maria Marinelli, Gabriele Tonni, Monia Rinaldini
Publikováno v:
Fetal and Pediatric Pathology. 41:299-305
Background: Mosaic trisomy 12 is a genetic condition with few cases diagnosed prenatally and postnatally. Phenotypic variability is wide ranging from normal patients to severe congenital anomalies....
Autor:
Vincenza Ylenia Cusenza, Alessandra Bisagni, Monia Rinaldini, Raffaele Frazzi, Chiara Cattani
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 4732, p 4732 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 4732, p 4732 (2021)
The cytogenetic and molecular assessment of deletions, amplifications and rearrangements are key aspects in the diagnosis and therapy of cancer. Not only the initial evaluation and classification of the disease, but also the follow-up of the tumor re
Autor:
Giuseppina Comitini, Gabriele Tonni, Silvia Asioli, Monia Rinaldini, Veronica Barbieri, Maria Marinelli, Maria Paola Bonasoni
Publikováno v:
Fetal and pediatric pathology. 41(3)
Trisomy mosaicism of chromosome 5 is uncommon with few cases described. Case report: A 41-year-old woman underwent ultrasound (US) at 16 weeks, which showed oligohydramnios and intrauterine growth ...