G.P.302 by Peay, H.L, Scharff, H, Biesecker, B.B, Wilfond, B.S, Johnson, J, Escolar, D.M, Bowie, J, Nagaraju, K, Piacentino, J, Tibben, A

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G.P.303 by Peay, H.L, Scharff, H, Biesecker, B.B, Wilfond, B.S, Johnson, J, Escolar, D.M, Nagaraju, K, Piacentino, J, Bowie, J, Tibben, A

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Defining personal utility in genomics: A Delphi study by Kohler, J.N., Turbitt, E., Lewis, K.L., Wilfond, B.S., Jamal, L., Peay, H.L., Biesecker, L.G., Biesecker, B.B.

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Patient actions and reactions after receiving negative results from expanded carrier screening by Kraft, S.A., Schneider, J.L., Leo, M.C., Kauffman, T.L., Davis, J.V., Porter, K.M., McMullen, C.K., Wilfond, B.S., Goddard, K.A.B.

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Integrating neurocritical care approaches into neonatology: should all infants be treated equitably? by Mann, P C, Gospe, S M, Steinman, K J, Wilfond, B S

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G.P.303: Influences on parental decision making about participation in Duchenne and Becker muscular dystrophy clinical trials by Peay, H.L., Scharff, H., Biesecker, B.B., Wilfond, B.S., Johnson, J., Escolar, D.M., Nagaraju, K., Piacentino, J., Bowie, J., Tibben, A.

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G.P.302: Perceived barriers and facilitators of participation in clinical trials for Duchenne and Becker muscular dystrophy by Peay, H.L., Scharff, H., Biesecker, B.B., Wilfond, B.S., Johnson, J., Escolar, D.M., Bowie, J., Nagaraju, K., Piacentino, J., Tibben, A.

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Patient Perspectives on Group Benefits and Harms in Genetic Research by Goldenberg, A.J., Hull, S.C., Wilfond, B.S., Sharp, R.R.

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Characterisation of organisational issues in paediatric clinical ethics consultation: a qualitative study by Opel, D J, Wilfond, B S, Brownstein, D, Diekema, D S, Pearlman, R A

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Disclosing individual genetic results to research participants by Ravitsky, V, Wilfond, B.S

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