Genetic Basis of Orthopedic Diseases
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-20777-3_14
Reference24 articles.
1. Benichou O, Cleiren E, Gram J (2001) Mapping of autosomal dominant osteopetrosis type II (Albers-Schonberg disease) to chromosome 16p13.3. Am J Hum Genet 69:647–654
2. Childs B (1982) Genetics in the medical curriculum. Am J Med Genet 13:319–324
3. Cleiren E, Benichou O, Van Hul E (2001) Albers-Schonberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene. Hum Mol Genet 10:2861–2867
4. Colbert RA (2007) Skeletal disorders. Genes and common diseases. Genetics in modern medicine by Alan Wright and Nicholas Hastie. Cambridge University Press, Cambridge, UK
5. Cooper GS, Umbach DM (1996) Are vitamin D receptor polymorphism associated with bone mineral density? A meta-analysis. J Bone Miner Res 11:1841–1849
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