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 diagnosed...

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Autors principals:	Haoran Mu, Yafei Jiang, Linghang Xue, Yingqi Hua, Jun Lin, Zhengdong Cai
Format:	Artigo
Idioma:	Inglês
Publicat:	Wiley 2021-04-01
Col·lecció:	Orthopaedic Surgery
Matèries:	Chondroblastoma Chondromyxoid fibroma Giant‐cell tumor of bone Histone H3K36 mutation Immunohistochemistry
Accés en línia:	https://doi.org/10.1111/os.12878
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