H3.3 K36M Mutation as a Clinical Diagnosis Method of Suspected Chondroblastoma Cases

OBJECTIVE: Whether H3.3 K36M mutation (H3K36M) could be an approach if the diagnosis of chondroblastoma (CB) patients was indistinct and it was suspected to be unclear clinically. METHODS: We reviewed and compared our clinical experiences of CB cases and some suspected cases, which were not diagnose...

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Detalles Bibliográficos
Autores principales: Mu, Haoran, Jiang, Yafei, Xue, Linghang, Hua, Yingqi, Lin, Jun, Cai, Zhengdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2021
Materias:
Scientific Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7957386/
https://www.ncbi.nlm.nih.gov/pubmed/33620145
http://dx.doi.org/10.1111/os.12878

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7957386/
https://www.ncbi.nlm.nih.gov/pubmed/33620145
http://dx.doi.org/10.1111/os.12878

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