Associated Papers
CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and Limitations.
Royer-Bertrand B et al.
Genes, 2021
34573409 (PubMed )
Supplement: genes-12-01427-s001.zip › Table_S4_Royer-Bertrand_Revision.pdf
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