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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Detalles Bibliográficos
Autores principales: Jamsheer, Aleksander, Socha, Magdalena, Sowińska-Seidler, Anna, Telega, Kinga, Trzeciak, Tomasz, Latos-Bieleńska, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Human Genetics • Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990859/
https://www.ncbi.nlm.nih.gov/pubmed/24532482
http://dx.doi.org/10.1007/s13353-014-0195-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990859/
https://www.ncbi.nlm.nih.gov/pubmed/24532482
http://dx.doi.org/10.1007/s13353-014-0195-z

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