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Van Buchem Disease (Hyperostosis Corticalis Generalisata) Maps to Chromosome 17q12-q21 - ScienceDirect
Localization of the Gene for Sclerosteosis to the van Buchem Disease–Gene Region on Chromosome 17q12–q21 - ScienceDirect
Case 150: Van Buchem Disease (Hyperostosis Corticalis Generalisata) | Radiology
Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease | Journal of Medical Genetics
Case 150: Van Buchem disease (hyperostosis corticalis generalisata). | Semantic Scholar
High bone formation | International Osteoporosis Foundation
Van Buchem disease: lifetime evolution of radioclinical features | SpringerLink
PDF] Skallagrímsson : The first case of Van Buchem disease ? | Semantic Scholar
Localization of the Gene for Sclerosteosis to the van Buchem Disease–Gene Region on Chromosome 17q12–q21 - ScienceDirect
Sclerostin: Current Knowledge and Future Perspectives | SpringerLink
Van Buchem Disease (Hyperostosis Corticalis Generalisata) Maps to Chromosome 17q12-q21 - ScienceDirect
Clinical effects of sclerosteosis and van Buchem disease. Notes: (A)... | Download Scientific Diagram
Van Buchem disease: First case report in Taiwan. - Abstract - Europe PMC
Van Buchem disease: A rare sclerosing dysplasia - Indian Journal of Musculoskeletal Radiology (IJMSR)
Clinical representation of patients with sclerosteosis and van Buchem... | Download Scientific Diagram
The syndromic status of sclerosteosis and van Buchem disease
Van Buchem disease | Radiology Reference Article | Radiopaedia.org
The syndromic status of sclerosteosis and van Buchem disease
Van Buchem disease | Eurorad
A rare cause of facial nerve palsy in children: Hyperostosis corticalis generalisata (Van Buchem disease). Three new pediatric c
Van Buchem disease | Eurorad
Van Buchem Disease, Sclerosteosis or Something Else? | SpringerLink
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