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    Boer, C., Narcisi, R., Ramos, Y., Hollander, W. d., Bomer, N., Betancourt, M. C., Uitterlinden, A., van Osch, G., Meulenbelt, I., & van Meurs, J. (n.d.). genetic variants in the SUPT3H-RUNX2 locus confer susceptibility for bone and cartilage related disorders via long-range regulation of RUNX2. Osteoarthritis and cartilage, 23, A71–. http://access.bl.uk/ark:/81055/vdc_100059823707.0x000001
  
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