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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Bone Miner Res
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: 2018
Matèries:
Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars