Van Buchem Disease (Hyperostosis Corticalis Generalisata) Maps to Chromosome 17q12-q21
β Scribed by Wim Van Hul; Wendy Balemans; Els Van Hul; Frederik G. Dikkers; Henk Obee; Robert J. Stokroos; Peter Hildering; Filip Vanhoenacker; Guy Van Camp; Patrick J. Willems
- Book ID
- 117852296
- Publisher
- American Society of Human Genetics
- Year
- 1998
- Tongue
- English
- Weight
- 736 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0002-9297
- DOI
- 10.1086/301721
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π SIMILAR VOLUMES
Familial frontotemporal dementia (FTD) is a complex disorder with lack of distinctive histopathological markers found in other types of dementia. Most of the linkage reports from FTD families map the disease loci to chromosome 17q21-22. However, FTD is genetically heterogeneous, as linkage also has
## Abstract Van Buchem disease is an autosomal recessive sclerosing bone dysplasia characterized by skeletal hyperostosis, overgrowth of the mandible, and a liability to entrapment of the seventh and eighth cranial nerves. The genetic determinant maps to chromosome 17q12βq21. We refined the critica