Bell, P. A., Piróg, K. A., Fresquet, M., Thornton, D. J., Boot-Handford, R. P., & Briggs, M. D. (2012). Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation. Wiley Subscription Services, Inc., A Wiley Company.

Bell, Peter A., Katarzyna A. Piróg, Maryline Fresquet, David J. Thornton, Raymond P. Boot-Handford, and Michael D. Briggs. Loss of Matrilin 1 Does Not Exacerbate the Skeletal Phenotype in a Mouse Model of Multiple Epiphyseal Dysplasia Caused By a Matn3 V194D Mutation. Wiley Subscription Services, Inc., A Wiley Company, 2012.

Bell, Peter A., et al. Loss of Matrilin 1 Does Not Exacerbate the Skeletal Phenotype in a Mouse Model of Multiple Epiphyseal Dysplasia Caused By a Matn3 V194D Mutation. Wiley Subscription Services, Inc., A Wiley Company, 2012.