Items where authors include "Fratzl-Zelman, N."

Article

Balasubramanian, M. orcid.org/0000-0003-1488-3695, Fratzl-Zelman, N., O'Sullivan, R. et al. (9 more authors) (2018) Novel PLS3 variants in X-linked osteoporosis: Exploring bone material properties. American Journal of Medical Genetics Part A, 176 (7). pp. 1578-1586. ISSN 1552-4825

Marini, J.C., Forlino, A., Bächinger, H.P. et al. (9 more authors) (2017) Osteogenesis imperfecta. Nature Reviews: Disease Primers, 3. 17052. ISSN 2056-676X

Webb, E.A., Balasubramanian, M., Fratzl-Zelman, N. et al. (16 more authors) (2017) Phenotypic spectrum in osteogenesis imperfecta due to mutations in TMEM38B: unravelling a complex cellular defect. Journal of Clinical Endocrinology and Metabolism, 102 (6). pp. 2019-2028. ISSN 0021-972X