1. A Novel EXT1 Mutation Identified in a Family with Multiple Osteochondromas
   Zhonghua Chen et al, 2019, Genetic Testing and Molecular Biomarkers CrossRef
2. Identification of Novel Mutations in the EXT1 and EXT2 Genes of Chinese Patients with Hereditary Multiple Osteochondromas
   Yu Tong et al, 2021, Genetic Testing and Molecular Biomarkers CrossRef
3. Identification of a rare case of intra-articular osteochondroma manifesting as three loose bodies in a patient with hereditary multiple osteochondromas: A case report
   MINGXIANG KONG et al, 2015, Oncology Letters CrossRef
4. RNA‐Seq detects a SAMD12‐EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromas
   Gavin R. Oliver et al, 2019, Molecular Genetics & Genomic Medicine CrossRef
5. A Novel Nonsense Mutation in the EXT2 Gene Identified in a Family with Hereditary Multiple Osteochondromas
   Zhonghua Chen et al, 2020, Genetic Testing and Molecular Biomarkers CrossRef
6. Haploinsufficiency of EXT1 and Heparan Sulphate Deficiency Associated with Hereditary Multiple Exostoses in a Pakistani Family
   Muhammad Ajmal et al, 2022, Medicina CrossRef
7. Mutant EXT1 in Taiwanese Patients with Multiple Hereditary Exostoses
   Wei-De Lin et al, 2014, BioMedicine CrossRef
8. Novel exostosin-2 mutation identified in a Chinese family with hereditary multiple osteochondroma
   Weiwei Ruan et al, 2018, Oncology Letters CrossRef