Search Results - Werner Lin
- Showing 1 - 18 results of 18
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‘My funky genetics’: BRCA1/2 mutation carriers’ understanding of genetic inheritance and reproductive merger in the context of new repro-genetic technologies by Werner-Lin, Allison, Rubin, Lisa R., Doyle, Maya, Stern, Rikki, Savin, Katie, Hurley, Karen, Sagi, Michal
Published 2012Text -
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Waiting and “weighted down”: the challenge of anticipatory loss for individuals and families with Li‑Fraumeni Syndrome by Werner‑Lin, Allison, Young, Jennifer L., Wilsnack, Catherine, Merrill, Shana L., Groner, Victoria, Greene, Mark H., Khincha, Payal P.
Published 2020Text -
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Incorporating information about pre-implantation genetic diagnosis into discussions about testing and risk-management for BRCA1/2 mutations: A qualitative study of patient preferen... by Hurley, Karen, Rubin, Lisa, Werner-Lin, Allison, Sagi, Michal, Kemel, Yelena, Stern, Rikki, Phillips, Aliza, Cholst, Ina, Kauff, Noah, Offit, Kenneth
Published 2012Text -
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Family Identity and Roles in the Context of Li-Fraumeni Syndrome: “No One’s Like Us Mutants” by Wilsnack, Catherine, Young, Jennifer L., Merrill, Shana L., Groner, Victoria, Loud, Jennifer T., Bremer, Renee C., Greene, Mark H., Khincha, Payal P., Werner-Lin, Allison
Published 2021Text -
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Couples coping with screening burden and diagnostic uncertainty in Li-Fraumeni syndrome: Connection versus independence by Young, Jennifer L., Pantaleao, Ashley, Zaspel, Lori, Bayer, Jessica, Peters, June A., Khincha, Payal P., Bremer, Renee C., Loud, Jennifer T., Greene, Mark H., Achatz, Maria Isabel, Savage, Sharon A., Werner-Lin, Allison
Published 2018Text -
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Family Health Leaders: Lessons on Living with Li-Fraumeni Syndrome across Generations by PANTALEAO, ASHLEY, YOUNG, JENNIFER L., EPSTEIN, NORMAN B., CARLSON, MAE, BREMER, RENÉE C., KHINCHA, PAYAL P., PETERS, JUNE A., GREENE, MARK H., ROY, KEVIN, ACHATZ, MARIA ISABEL, SAVAGE, SHARON A., WERNER-LIN, ALLISON
Published 2019Text
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