Comprehensive reanalysis for CNVs in exome sequencing data from unsolved rare disease cases results in new diagnoses
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L. Vissers | A. Hoischen | C. Gilissen | G. Demidov | I. Paramonov | L. Johansson | B. Yaldiz | S. Laurie | José Garcia-Pelaez | Elisa Benetti | Nika Schuermans | Katja Lohmann | S. Beltrán | R. D. Voer | Stephan Ossowski | Gemma Bullich | Karolis Sablauskas | Elke de Boer | L. V. D. Vondel | Francesco Musacchia | Carla Oliveira | Ana Topf | Solve-RD Consortia