The high bone mass phenotype is characterised by a combined cortical and trabecular bone phenotype: Findings from a pQCT case–control study()

High bone mass (HBM), detected in 0.2% of DXA scans, is characterised by a mild skeletal dysplasia largely unexplained by known genetic mutations. We conducted the first systematic assessment of the skeletal phenotype in unexplained HBM using pQCT in our unique HBM population identified from screeni...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Gregson, Celia L., Sayers, Adrian, Lazar, Victor, Steel, Sue, Dennison, Elaine M., Cooper, Cyrus, Smith, George Davey, Rittweger, Jörn, Tobias, Jon H.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier Science 2013
Aiheet:
Original Full Length Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3526774/
https://ncbi.nlm.nih.gov/pubmed/23103330
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2012.10.021
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