CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and Limitations
Béryl Royer‐Bertrand(University of Lausanne), Andrea Superti‐Furga(University of Lausanne), Lauréane Mittaz‐Crettol(University of Lausanne), Florence Niel‐Bütschi(University of Lausanne), Heidi Fodstad(University of Lausanne), Katarina Cisarova(University of Lausanne)
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