Royer-Bertrand, B.; Cisarova, K.; Niel-Butschi, F.; Mittaz-Crettol, L.; Fodstad, H.; Superti-Furga, A.
CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and Limitations. Genes 2021, 12, 1427.
https://doi.org/10.3390/genes12091427
AMA Style
Royer-Bertrand B, Cisarova K, Niel-Butschi F, Mittaz-Crettol L, Fodstad H, Superti-Furga A.
CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and Limitations. Genes. 2021; 12(9):1427.
https://doi.org/10.3390/genes12091427
Chicago/Turabian Style
Royer-Bertrand, Beryl, Katarina Cisarova, Florence Niel-Butschi, Laureane Mittaz-Crettol, Heidi Fodstad, and Andrea Superti-Furga.
2021. "CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and Limitations" Genes 12, no. 9: 1427.
https://doi.org/10.3390/genes12091427
APA Style
Royer-Bertrand, B., Cisarova, K., Niel-Butschi, F., Mittaz-Crettol, L., Fodstad, H., & Superti-Furga, A.
(2021). CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and Limitations. Genes, 12(9), 1427.
https://doi.org/10.3390/genes12091427