Papers: 10.3390/genes12091427
https://doi.org/10.3390/genes12091427
CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and Limitations
Cited by: 14
Author(s): Béryl Royer‐Bertrand, Katarina Cisarova, Florence Niel-Bütschi, Lauréane Mittaz-Crettol, Heidi Fodstad, Andrea Superti‐Furga
Published: almost 4 years ago
Software Mentions 1
Very Likely Science (75)