Van Buchem disease (hyperostosis corticalis generalisata) maps to chromosome 17q12-q21.

Van Buchem disease (hyperostosis corticalis generalisata; OMIM 239100 [http://www3.ncbi.nlm.nih. gov:80/htbin-post/Omim/dispmim?239100]) is an autosomal recessive disorder characterized by hyperostosis of the skull, mandible, clavicles, ribs, and diaphyseal cortices of the long bones. The most strik...

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Bibliografiske detaljer
Main Authors: Van Hul, W, Balemans, W, Van Hul, E, Dikkers, F G, Obee, H, Stokroos, R J, Hildering, P, Vanhoenacker, F, Van Camp, G, Willems, P J
Format: Artigo
Sprog:Inglês
Udgivet: 1998
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1376897/
https://ncbi.nlm.nih.gov/pubmed/9463328
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