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Molina-Ramírez LP, Kyle C, Ellingford JM, et al. Personalised virtual gene panels reduce interpretation workload and maintain diagnostic rates of proband-only clinical exome sequencing for rare disorders. J Med Genet. 2021;doi: 10.1136/jmedgenet-2020-107303.
Molina-Ramírez, L. P., Kyle, C., Ellingford, J. M., Wright, R., Taylor, A., Bhaskar, S. S., Campbell, C., Jackson, H., Fairclough, A., Rousseau, A., Burghel, G. J., Dutton, L., Banka, S., Briggs, T. A., Clayton-Smith, J., Douzgou, S., Jones, E. A., Kingston, H. M., Kerr, B., Ealing, J., Somarathi, S., Chandler, K. E., Stuart, H. M., Burkitt-Wright, E. M., Newman, W. G., Bruce, I. A., Black, G. C., & Gokhale, D. (2021). Personalised virtual gene panels reduce interpretation workload and maintain diagnostic rates of proband-only clinical exome sequencing for rare disorders. Journal of medical genetics, . https://doi.org/10.1136/jmedgenet-2020-107303
Molina-Ramírez, Leslie Patricia, et al. "Personalised virtual gene panels reduce interpretation workload and maintain diagnostic rates of proband-only clinical exome sequencing for rare disorders." Journal of medical genetics vol. (2021). doi: https://doi.org/10.1136/jmedgenet-2020-107303
Molina-Ramírez LP, Kyle C, Ellingford JM, Wright R, Taylor A, Bhaskar SS, Campbell C, Jackson H, Fairclough A, Rousseau A, Burghel GJ, Dutton L, Banka S, Briggs TA, Clayton-Smith J, Douzgou S, Jones EA, Kingston HM, Kerr B, Ealing J, Somarathi S, Chandler KE, Stuart HM, Burkitt-Wright EM, Newman WG, Bruce IA, Black GC, Gokhale D. Personalised virtual gene panels reduce interpretation workload and maintain diagnostic rates of proband-only clinical exome sequencing for rare disorders. J Med Genet. 2021 Apr 20; doi: 10.1136/jmedgenet-2020-107303. Epub 2021 Apr 20. PMID: 33879512.
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