How do consent forms for diagnostic high‐throughput sequencing address unsolicited and secondary findings? A content analysis von Vears, D.F., Niemiec, E., Howard, H.C., Borry, P.

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Should we respect parents' views about which results to return from genomic sequencing? von Vears, D.F

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SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure von Dibbens, L.M., Michelucci, R., Gambardella, A., Andermann, F., Rubboli, G., Bayly, M.A., Joensuu, T., Vears, D.F., Franceschetti, S., Canafoglia, L., Wallace, R., Bassuk, A.G., Power, D.A., Tassinari, C.A., Andermann, E., Lehesjoki, A.E., Berkovic, S.F.

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A Systematic Analysis of Online Marketing Materials Used by Providers of Expanded Carrier Screening von Chokoshvili, D, Borry, P, Vears, D.F

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Navigating the uncertainties of next-generation sequencing in the genetics clinic von Kuiper, J.M.L, Borry, Pascal, Vears, D.F, Van Esch, Hilde, Van Hoyweghen, Ine

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How do consent forms for diagnostic high-throughput sequencing address unsolicited and secondary findings? A content analysis von Vears, D.F, Niemiec, E, Howard, H.C, Borry, P

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The patient with 41 reports: analysis of laboratory exome sequencing reporting of a "virtual patient" von Vears, D.F., Elferink, M., Kriek, M., Borry, P., Gassen, K.L. van

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Analysis of laboratory reporting practices using a quality assessment of a virtual patient von Vears, D.F., Elferink, M., Kriek, M., Borry, P., Gassen, K.L. van

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