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Mutational Analysis of EXT1in a Chinese Family Affected by Hereditary Multiple Osteochondroma
OBJECTIVES: To discuss the mutational features and their relationships with disease in a family with hereditary multiple osteochondroma (HMO) from Guangxi Province (GXBB-1 family), China. METHODS: Genomic DNA and total mRNA were extracted from peripheral blood cells of GXBB-1 family members. Whole e...
Autores principales: | Yuan, Guangzhi, Su, Qiang, Liao, Wenjun, Hou, Wei, Huang, Linke, Wang, Peng, Wu, Huayu |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8367584/ https://www.ncbi.nlm.nih.gov/pubmed/34409107 http://dx.doi.org/10.1155/2021/8888948 |
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