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RNA Panel Sequencing Is an Effective Tool to Help Classify Splice Variants for Clinical Oncogenetic Diagnosis

Document Type

Article

Author

Privat, M.; Ponelle-Chachuat, F.; Viala, S.; Uhrhammer, N.; Lepage, M.; Cayre, A.; Bidet, Y.; Bignon, Y.-J.; Gay-Bellile, M.; Cavaillé, M.

Source

In: Human Mutation. (Human Mutation, 2024, 2024)

Subject

Language

English

ISSN

10981004
10597794

Online Access

Full Text (Wiley Journals) Open Access (Wiley) Web of Science JCR 저널정보 Scopus Find it@PNU

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