Alvarez, CM; De Vera, MA; Heslip, TR; Casey, B (setembro de 2007). «Evaluation of the anatomic burden of patients with hereditary multiple exostoses.». Clin Orthop Relat Res. 462: 73–79. PMID17589361. doi:10.1097/BLO.0b013e3181334b51
Darilek S, Wicklund C, Novy D, Scott A, Gambello M, Johnston D, Hecht J (maio de 2005). «Hereditary multiple exostosis and pain». Journal of Pediatric Orthopedy. 25 (3): 369–76. PMID15832158. doi:10.1097/01.bpo.0000150813.18673.ad
Wu YQ, Heutink P, de Vries BB, Sandkuijl LA, van den Ouweland AM, Niermeijer MF, Galjaard H, Reyniers E, Willems PJ, Halley DJ (1994). «Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11». Human Molecular Genetics. 3 (1): 167–71. PMID8162019. doi:10.1093/hmg/3.1.167
Le Merrer M, Legeai-Mallet L, Jeannin PM, Horsthemke B, Schinzel A, Plauchu H, Toutain A, Achard F, Munnich A, Maroteaux P (1994). «A gene for hereditary multiple exostoses maps to chromosome 19p». Human Molecular Genetics. 3 (5): 717–22. CiteSeerX10.1.1.1028.5356. PMID8081357. doi:10.1093/hmg/3.5.717
Zak BM, Crawford BE, Esko JD (2002). «Hereditary multiple exostoses and heparan sulfate polymerization». Biochimica et Biophysica Acta (BBA) - General Subjects. 1573 (3): 346–55. PMID12417417. doi:10.1016/S0304-4165(02)00402-6
Stieber JR, Dormans JP (2005). «Manifestations of hereditary multiple exostoses». The Journal of the American Academy of Orthopaedic Surgeons. 13 (2): 110–20. PMID15850368. doi:10.5435/00124635-200503000-00004
Legeai-Mallet L, Munnich A, Maroteaux P, Le Merrer M (julho de 1997). «Incomplete penetrance and expressivity skewing in hereditary multiple exostoses». Clinical Genetics. 52 (1): 12–6. PMID9272707. doi:10.1111/j.1399-0004.1997.tb02508.x
Faiyaz-Ul-Haque M, Ahmad W, Zaidi SH, et al. (agosto de 2004). «Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis)». Clinical Genetics. 66 (2): 144–51. PMID15253765. doi:10.1111/j.1399-0004.2004.00275.x
Porter DE, Lonie L, Fraser M, et al. (setembro de 2004). «Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype study». The Journal of Bone and Joint Surgery. British Volume. 86 (7): 1041–6. PMID15446535. doi:10.1302/0301-620x.86b7.14815|hdl-access= requer |hdl= (ajuda)
Kivioja A, Ervasti H, Kinnunen J, Kaitila I, Wolf M, Böhling T (março de 2000). «Chondrosarcoma in a family with multiple hereditary exostoses». The Journal of Bone and Joint Surgery. British Volume. 82 (2): 261–6. PMID10755438. doi:10.1302/0301-620X.82B2.0820261
Parada Duarte O, Arambula Neira J, Castillo Herazo V, Oviedo Lara M, López Polanco A, Durán Omaña A, Herrera Ortiz AF. Popliteal artery pseudoaneurysm caused by non–penetrating trauma in a patient with hereditary multiple osteochondromatosis. Radiology Case Reports.2021;17(1):185-189. https://doi.org/10.1016/j.radcr.2021.10.025
Wuyts, W; Schmale, GA; Chansky, HA; et al. (21 de novembro de 2013). «Hereditary Multiple Osteochondromas.». University of Washington, Seattle. GeneReviews. PMID20301413. Consultado em 24 de março de 2018
Alvarez, CM; De Vera, MA; Heslip, TR; Casey, B (setembro de 2007). «Evaluation of the anatomic burden of patients with hereditary multiple exostoses.». Clin Orthop Relat Res. 462: 73–79. PMID17589361. doi:10.1097/BLO.0b013e3181334b51
Darilek S, Wicklund C, Novy D, Scott A, Gambello M, Johnston D, Hecht J (maio de 2005). «Hereditary multiple exostosis and pain». Journal of Pediatric Orthopedy. 25 (3): 369–76. PMID15832158. doi:10.1097/01.bpo.0000150813.18673.ad
Wu YQ, Heutink P, de Vries BB, Sandkuijl LA, van den Ouweland AM, Niermeijer MF, Galjaard H, Reyniers E, Willems PJ, Halley DJ (1994). «Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11». Human Molecular Genetics. 3 (1): 167–71. PMID8162019. doi:10.1093/hmg/3.1.167
Le Merrer M, Legeai-Mallet L, Jeannin PM, Horsthemke B, Schinzel A, Plauchu H, Toutain A, Achard F, Munnich A, Maroteaux P (1994). «A gene for hereditary multiple exostoses maps to chromosome 19p». Human Molecular Genetics. 3 (5): 717–22. CiteSeerX10.1.1.1028.5356. PMID8081357. doi:10.1093/hmg/3.5.717
Zak BM, Crawford BE, Esko JD (2002). «Hereditary multiple exostoses and heparan sulfate polymerization». Biochimica et Biophysica Acta (BBA) - General Subjects. 1573 (3): 346–55. PMID12417417. doi:10.1016/S0304-4165(02)00402-6
Stieber JR, Dormans JP (2005). «Manifestations of hereditary multiple exostoses». The Journal of the American Academy of Orthopaedic Surgeons. 13 (2): 110–20. PMID15850368. doi:10.5435/00124635-200503000-00004
Legeai-Mallet L, Munnich A, Maroteaux P, Le Merrer M (julho de 1997). «Incomplete penetrance and expressivity skewing in hereditary multiple exostoses». Clinical Genetics. 52 (1): 12–6. PMID9272707. doi:10.1111/j.1399-0004.1997.tb02508.x
Faiyaz-Ul-Haque M, Ahmad W, Zaidi SH, et al. (agosto de 2004). «Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis)». Clinical Genetics. 66 (2): 144–51. PMID15253765. doi:10.1111/j.1399-0004.2004.00275.x
Porter DE, Lonie L, Fraser M, et al. (setembro de 2004). «Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype study». The Journal of Bone and Joint Surgery. British Volume. 86 (7): 1041–6. PMID15446535. doi:10.1302/0301-620x.86b7.14815|hdl-access= requer |hdl= (ajuda)
Kivioja A, Ervasti H, Kinnunen J, Kaitila I, Wolf M, Böhling T (março de 2000). «Chondrosarcoma in a family with multiple hereditary exostoses». The Journal of Bone and Joint Surgery. British Volume. 82 (2): 261–6. PMID10755438. doi:10.1302/0301-620X.82B2.0820261
Le Merrer M, Legeai-Mallet L, Jeannin PM, Horsthemke B, Schinzel A, Plauchu H, Toutain A, Achard F, Munnich A, Maroteaux P (1994). «A gene for hereditary multiple exostoses maps to chromosome 19p». Human Molecular Genetics. 3 (5): 717–22. CiteSeerX10.1.1.1028.5356. PMID8081357. doi:10.1093/hmg/3.5.717