Correction: Identity development and adaptation in adolescents with genetic conditions: a qualitatively oriented mixed-methods study to develop strategies for optimizing clinical genetics services.

IF 3.5 2区医学 Q2 GENETICS & HEREDITY

Orphanet Journal of Rare Diseases Pub Date : 2025-09-18 DOI:10.1186/s13023-025-04023-5

Tasha Wainstein, Cyrus Boelman, Connie Ens, William T Gibson, Kevin Gregory-Evans, Olubayo U Kolawole, Sheila K Marshall, Kathryn Selby, Jehannine Austin, Alison M Elliott

引用次数: 0

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纠正：有遗传条件的青少年的身份发展和适应：一项以定性为导向的混合方法研究，以制定优化临床遗传学服务的策略。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Orphanet Journal of Rare Diseases 医学-医学：研究与实验

CiteScore

6.30

自引率

8.10%

发文量

418

审稿时长

4-8 weeks

期刊介绍： Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.