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pro vyhledávání: '"Medical Genome Committee"'
Autor:
China Alliance for Rare Diseases, Beijing Society of Rare Disease Clinical Care and Accessibility, Medical Genome Committee
Publikováno v:
罕见病研究, Vol 3, Iss 3, Pp 275-279 (2024)
With the development of medical genomics, whole genome sequencing (WGS) has been playing an increasingly important role in the diagnosis and treatment of rare diseases. To effectively promote the application of WGS in clinical diagnosis and treatment
Externí odkaz:
https://doaj.org/article/cad63ca6ad8b4f6fa6073e7ed53c5cc1
