Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Stefania Maccarini"'
Autor:
Eleonora Marchina, Michela Forti, Mariella Tonelli, Stefania Maccarini, Francesca Malvestiti, Chiara Piantoni, Elena Filippini, Elisa Fazzi, Giuseppe Borsani
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-8 (2021)
Abstract Background Small supernumerary marker chromosomes (sSMC) are a heterogeneous group of structurally abnormal chromosomes, with an incidence of 0,044% in newborns that increases up to almost 7 times in developmentally retarded patients. sSMC f
Externí odkaz:
https://doaj.org/article/60680abd01ed4a68bb010ea73d146dc3
Autor:
Stefania Maccarini, Annamaria Cipani, Valeria Bertini, Jelena Skripac, Alessandro Salvi, Giuseppe Borsani, Eleonora Marchina
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-8 (2020)
Abstract Background Tourette syndrome (TS) is a complex neurodevelopmental disorder (NDD) characterized by multiple chronic involuntary motor and vocal tics with onset during childhood or adolescence. Most TS patients present with additional comorbid
Externí odkaz:
https://doaj.org/article/a35a8f162cbc4fd1b5df737e649c4505
Autor:
Chiara Piantoni, Stefania Maccarini, Francesca Malvestiti, Elena Filippini, Eleonora Marchina, Elisa Fazzi, Giuseppe Borsani, Michela Forti, Mariella Tonelli
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-8 (2021)
Molecular Cytogenetics
Molecular Cytogenetics
Background Small supernumerary marker chromosomes (sSMC) are a heterogeneous group of structurally abnormal chromosomes, with an incidence of 0,044% in newborns that increases up to almost 7 times in developmentally retarded patients. sSMC from all 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1998e2d23ff8c1e49000b9d2868751e
https://doaj.org/article/60680abd01ed4a68bb010ea73d146dc3
https://doaj.org/article/60680abd01ed4a68bb010ea73d146dc3