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Mutational screening of EXT1 and EXT2 genes in Polish patients with hereditary multiple exostoses
Hereditary multiple exostoses (HME) also known as multiple osteochondromas represent one of the most frequent bone tumor disorder in humans. Its clinical presentation is characterized by the presence of multiple benign cartilage-capped tumors located most commonly in the juxta-epiphyseal portions of...
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| Huvudupphovsmän: | , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Springer Berlin Heidelberg
2014
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3990859/ https://ncbi.nlm.nih.gov/pubmed/24532482 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13353-014-0195-z |
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