Privitera, F.; Calonaci, A.; Doddato, G.; Papa, F.T.; Baldassarri, M.; Pinto, A.M.; Mari, F.; Longo, I.; Caini, M.; Galimberti, D.;
et al. 13q Deletion Syndrome Involving RB1: Characterization of a New Minimal Critical Region for Psychomotor Delay. Genes 2021, 12, 1318.
https://doi.org/10.3390/genes12091318
AMA Style
Privitera F, Calonaci A, Doddato G, Papa FT, Baldassarri M, Pinto AM, Mari F, Longo I, Caini M, Galimberti D,
et al. 13q Deletion Syndrome Involving RB1: Characterization of a New Minimal Critical Region for Psychomotor Delay. Genes. 2021; 12(9):1318.
https://doi.org/10.3390/genes12091318
Chicago/Turabian Style
Privitera, Flavia, Arianna Calonaci, Gabriella Doddato, Filomena Tiziana Papa, Margherita Baldassarri, Anna Maria Pinto, Francesca Mari, Ilaria Longo, Mauro Caini, Daniela Galimberti,
and et al. 2021. "13q Deletion Syndrome Involving RB1: Characterization of a New Minimal Critical Region for Psychomotor Delay" Genes 12, no. 9: 1318.
https://doi.org/10.3390/genes12091318
APA Style
Privitera, F., Calonaci, A., Doddato, G., Papa, F. T., Baldassarri, M., Pinto, A. M., Mari, F., Longo, I., Caini, M., Galimberti, D., Hadjistilianou, T., De Francesco, S., Renieri, A., & Ariani, F.
(2021). 13q Deletion Syndrome Involving RB1: Characterization of a New Minimal Critical Region for Psychomotor Delay. Genes, 12(9), 1318.
https://doi.org/10.3390/genes12091318
