P383: Genetic counseling for clinical sequencing: Addressing variants of uncertain significance in rare disease diagnosis
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| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2025-01-01
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| Series: | Genetics in Medicine Open |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2949774425003875 |
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| _version_ | 1850139223758209024 |
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| author | Sumin Ji Hyon Kim |
| author_facet | Sumin Ji Hyon Kim |
| author_sort | Sumin Ji |
| collection | DOAJ |
| format | Article |
| id | doaj-art-8f8f23367d6b44c6bffb1b86aecbceaf |
| institution | OA Journals |
| issn | 2949-7744 |
| language | English |
| publishDate | 2025-01-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Genetics in Medicine Open |
| spelling | doaj-art-8f8f23367d6b44c6bffb1b86aecbceaf2025-08-20T02:30:23ZengElsevierGenetics in Medicine Open2949-77442025-01-01310234810.1016/j.gimo.2025.102348P383: Genetic counseling for clinical sequencing: Addressing variants of uncertain significance in rare disease diagnosisSumin Ji0Hyon Kim1Korean Foundation of Rare DiseaseKorean Foundation of Rare Diseasehttp://www.sciencedirect.com/science/article/pii/S2949774425003875 |
| spellingShingle | Sumin Ji Hyon Kim P383: Genetic counseling for clinical sequencing: Addressing variants of uncertain significance in rare disease diagnosis Genetics in Medicine Open |
| title | P383: Genetic counseling for clinical sequencing: Addressing variants of uncertain significance in rare disease diagnosis |
| title_full | P383: Genetic counseling for clinical sequencing: Addressing variants of uncertain significance in rare disease diagnosis |
| title_fullStr | P383: Genetic counseling for clinical sequencing: Addressing variants of uncertain significance in rare disease diagnosis |
| title_full_unstemmed | P383: Genetic counseling for clinical sequencing: Addressing variants of uncertain significance in rare disease diagnosis |
| title_short | P383: Genetic counseling for clinical sequencing: Addressing variants of uncertain significance in rare disease diagnosis |
| title_sort | p383 genetic counseling for clinical sequencing addressing variants of uncertain significance in rare disease diagnosis |
| url | http://www.sciencedirect.com/science/article/pii/S2949774425003875 |
| work_keys_str_mv | AT suminji p383geneticcounselingforclinicalsequencingaddressingvariantsofuncertainsignificanceinrarediseasediagnosis AT hyonkim p383geneticcounselingforclinicalsequencingaddressingvariantsofuncertainsignificanceinrarediseasediagnosis |