Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies.

Hereditary multiple exostoses (EXT) is an autosomal dominant disorder characterized by the formation of cartilage-capped prominences that develop from the growth centers of the long bones. EXT is genetically heterogeneous, with three loci, currently identified on chromosomes 8q24.1, 11p13, and 19q....

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Hlavní autoři: Hecht, J T, Hogue, D, Wang, Y, Blanton, S H, Wagner, M, Strong, L C, Raskind, W, Hansen, M F, Wells, D
Médium: Artigo
Jazyk:Inglês
Vydáno: 1997
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1712567/
https://ncbi.nlm.nih.gov/pubmed/8981950
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