Development of a storytelling communication facilitation tool (SCFT) to facilitate discussion of complex genetic diagnoses between parents and their children: A pilot study using 22q11.2 deletion syndrome as a model condition
开发一种叙事沟通促进工具（SCFT），以促进父母与子女之间关于复杂基因诊断的讨论：以22q11.2缺失综合征为模型疾病的试点研究
期刊:
影响因子:
doi:10.1016/j.pecinn.2022.100115
Bogatan, Simina; Shugar, Andrea; Wasim, Syed; Ball, Susan; Schmidt, Cathryn; Chitayat, David; Shuman, Cheryl; Cytrynbaum, Cheryl
