Multi-dimensional bone density phenotyping reveals new insights in to genetic regulation of the pediatric skeleton

Osteoporosis is a complex disease with developmental origins. It is therefore important to understand the genetic contribution to pediatric areal bone mineral density (aBMD). Individual skeletal site phenotyping has been primarily used to identify pediatric aBMD loci. However, this approach is limit...

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Bibliografiset tiedot
Julkaisussa:J Bone Miner Res
Päätekijät: Mitchell, Jonathan A., Chesi, Alessandra, Cousminer, Diana L., McCormack, Shana E., Kalkwarf, Heidi J., Lappe, Joan M., Gilsanz, Vicente, Oberfield, Sharon E., Shepherd, John A., Kelly, Andrea, Zemel, Babette S., Grant, Struan F.A.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2018
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7473448/
https://ncbi.nlm.nih.gov/pubmed/29240982
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbmr.3362
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