Sirica, R.; Ottaiano, A.; D’Amore, L.; Ianniello, M.; Petrillo, N.; Ruggiero, R.; Castiello, R.; Mori, A.; Evangelista, E.; De Falco, L.;
et al. Advancing Non-Invasive Prenatal Screening: A Targeted 1069-Gene Panel for Comprehensive Detection of Monogenic Disorders and Copy Number Variations. Genes 2025, 16, 427.
https://doi.org/10.3390/genes16040427
AMA Style
Sirica R, Ottaiano A, D’Amore L, Ianniello M, Petrillo N, Ruggiero R, Castiello R, Mori A, Evangelista E, De Falco L,
et al. Advancing Non-Invasive Prenatal Screening: A Targeted 1069-Gene Panel for Comprehensive Detection of Monogenic Disorders and Copy Number Variations. Genes. 2025; 16(4):427.
https://doi.org/10.3390/genes16040427
Chicago/Turabian Style
Sirica, Roberto, Alessandro Ottaiano, Luigi D’Amore, Monica Ianniello, Nadia Petrillo, Raffaella Ruggiero, Rosa Castiello, Alessio Mori, Eloisa Evangelista, Luigia De Falco,
and et al. 2025. "Advancing Non-Invasive Prenatal Screening: A Targeted 1069-Gene Panel for Comprehensive Detection of Monogenic Disorders and Copy Number Variations" Genes 16, no. 4: 427.
https://doi.org/10.3390/genes16040427
APA Style
Sirica, R., Ottaiano, A., D’Amore, L., Ianniello, M., Petrillo, N., Ruggiero, R., Castiello, R., Mori, A., Evangelista, E., De Falco, L., Santorsola, M., Misasi, M., Savarese, G., & Fico, A.
(2025). Advancing Non-Invasive Prenatal Screening: A Targeted 1069-Gene Panel for Comprehensive Detection of Monogenic Disorders and Copy Number Variations. Genes, 16(4), 427.
https://doi.org/10.3390/genes16040427
