Peltier, Leonard F. (January 1998). "A Case of Extraordinary Exostoses on the Back of a Boy". Clinical Orthopaedics and Related Research. 346: 5–6. doi:10.1097/00003086-199801000-00002. ISSN0009-921X.
Shore, Eileen M; Xu, Meiqi; Feldman, George J; Fenstermacher, David A; Cho, Tae-Joon; Choi, In Ho; Connor, J Michael; Delai, Patricia; Glaser, David L; LeMerrer, Martine; Morhart, Rolf; Rogers, John G; Smith, Roger; Triffitt, James T; Urtizberea, J Andoni; Zasloff, Michael; Brown, Matthew A; Kaplan, Frederick S (May 2006). "A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva". Nature Genetics. 38 (5): 525–527. doi:10.1038/ng1783. PMID16642017. S2CID41579747.
Lanchoney, TF; Cohen, RB; Rocke, DM; Zasloff, MA; Kaplan, FS (May 1995). "Permanent heterotopic ossification at the injection site after diphtheria-tetanus-pertussis immunizations in children who have fibrodysplasia ossificans progressiva". J Pediatr. 126 (5 Pt 1): 762–4. doi:10.1016/s0022-3476(95)70408-6. PMID7752003.
Shore, Eileen M; Xu, Meiqi; Feldman, George J; Fenstermacher, David A; Cho, Tae-Joon; Choi, In Ho; Connor, J Michael; Delai, Patricia; Glaser, David L; LeMerrer, Martine; Morhart, Rolf; Rogers, John G; Smith, Roger; Triffitt, James T; Urtizberea, J Andoni; Zasloff, Michael; Brown, Matthew A; Kaplan, Frederick S (May 2006). "A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva". Nature Genetics. 38 (5): 525–527. doi:10.1038/ng1783. PMID16642017. S2CID41579747.
Akesson, Lauren S.; Savarirayan, Ravi (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Fibrodysplasia Ossificans Progressiva", GeneReviews, Seattle (WA): University of Washington, Seattle, PMID32525643, retrieved 25 September 2025
Lanchoney, TF; Cohen, RB; Rocke, DM; Zasloff, MA; Kaplan, FS (May 1995). "Permanent heterotopic ossification at the injection site after diphtheria-tetanus-pertussis immunizations in children who have fibrodysplasia ossificans progressiva". J Pediatr. 126 (5 Pt 1): 762–4. doi:10.1016/s0022-3476(95)70408-6. PMID7752003.
Akesson, Lauren S.; Savarirayan, Ravi (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Fibrodysplasia Ossificans Progressiva", GeneReviews, Seattle (WA): University of Washington, Seattle, PMID32525643, retrieved 25 September 2025
Shore, Eileen M; Xu, Meiqi; Feldman, George J; Fenstermacher, David A; Cho, Tae-Joon; Choi, In Ho; Connor, J Michael; Delai, Patricia; Glaser, David L; LeMerrer, Martine; Morhart, Rolf; Rogers, John G; Smith, Roger; Triffitt, James T; Urtizberea, J Andoni; Zasloff, Michael; Brown, Matthew A; Kaplan, Frederick S (May 2006). "A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva". Nature Genetics. 38 (5): 525–527. doi:10.1038/ng1783. PMID16642017. S2CID41579747.
Peltier, Leonard F. (January 1998). "A Case of Extraordinary Exostoses on the Back of a Boy". Clinical Orthopaedics and Related Research. 346: 5–6. doi:10.1097/00003086-199801000-00002. ISSN0009-921X.