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You searched for: Author/Creator Robinson, Jill O.

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1. Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking families. Issue 5 (May 2019)

2. Conducting clinical genomics research during the COVID‐19 pandemic: Lessons learned from the CSER consortium experience. Issue 2 (7th November 2022)

3. Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression. Issue 1 (26th July 2021)

4. Examining access to care in clinical genomic research and medicine: Experiences from the CSER Consortium. Issue 1 (14th September 2021)

5. Exome sequencing disclosures in pediatric cancer care: Patterns of communication among oncologists, genetic counselors, and parents. Issue 4 (April 2019)

9. Lessons learned about harmonizing survey measures for the CSER consortium. Issue 6 (24th December 2020)

10. When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing. Issue 2 (3rd April 2017)