Copy number variants calling from WES data through eXome hidden Markov model (XHMM) identifies additional 2.5% pathogenic genomic imbalances smaller than 30 kb undetected by array‐CGH
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J. Thevenon | L. Faivre | C. Philippe | C. Thauvin-Robinet | Y. Duffourd | É. Tisserant | S. Moutton | P. Callier | S. Aho | N. Marle | P. Kuentz | M. Konyukh | A. Bruel | A. Mosca-Boidron | S. Nambot | M. Payet | C. Racine | J. Delanne | A. Sorlin | A. Vitobello | F. Tran-Mau-Them | Simon Verdez | D. Callegarin | Eleonore Viora-Dupont | A. Garde | Marlène Poulleau | C. Poé | Éléonore Viora-Dupont | Anne-Laure Mosca-Boidron | Marina Konyukh | É. Viora-Dupont