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Article

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

Orthopaedic surgery - 1 Apr 2021

Mu Haoran, Jiang Yafei, Xue Linghang, Hua Yingqi, Lin Jun, Cai Zhengdong

Abstract excerpt

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 distinctly, between 2013 to 2019. A total of 15 male and four female cases included in this study were seperated...

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Identifiers

PMID: 33620145
DOI: 10.1111/os.12878
PMCID: PMC7957386

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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H3.3 K36M Mutation as a Clinical Diagnosis Method of Suspected Chondroblastoma Cases.PMID 33620145Read ↗

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