Medical genetic counseling for patients with identified clinically significant genetic variants associated with hereditary tumor syndromes and their relatives
Медико-генетическое консультирование пациентов с выявленными клинически значимыми генетическими вариантами, ассоциированными с наследственными опухолевыми синдромами, и их родственников
2023-12-02
SCID: 54.1/r3xgvyxv
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clinically significant genetic variantshereditary tumor syndromesmedical genetic counselingrelatives (family members)
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Abstract (AI)
Индекс DOI для книги: Медико-генетическое консультирование пациентов с выявленными клинически значимыми генетическими вариантами, ассоциированными с наследственными опухолевыми синдромами, и их родственников
Key Findings
1
It addresses counseling practices specifically for individuals who have identified pathogenic or likely pathogenic variants associated with hereditary cancers
2
The content is intended to support both patients and their family members in understanding and managing hereditary cancer risk
3
The resource is presented as a book (monograph) providing guidance on genetic counseling in the context of hereditary tumor syndromes
4
The work focuses on medical genetic counseling for patients with clinically significant genetic variants linked to hereditary tumor syndromes and their relatives
Research Object
Medical genetic counseling for patients with identified clinically significant genetic variants associated with hereditary tumor syndromes and their relatives
Research Subject
Provision, content, and implications of medical genetic counseling (including risk communication, surveillance recommendations, cascade testing, and familial implications) for individuals carrying clinically significant pathogenic variants linked to hereditary cancer syndromes and their relatives
Publication Details
Publication Date
2023-12-02
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