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Published manuscripts on Hereditary multiple exostoses including 1992-1997 with links to the NCBI PubMed Database.

• Scarborough MT, et al. (1996) Benign cartilage tumors. Orthop Clin North Am. 27(3): 583-589.

• Atabay H, et al. (1996) Myelopathy due to hereditary multiple exostoses: CT and MR studies. Clin Neurol Neurosurg. 98(2): 186-188.

• Quirini GE, et al. (1996) Osteochondroma of the thoracic spine: an unusual cause of spinal cord compression. AJNR Am J Neuroradiol 17(5): 961-964.

• Stanton RP, et al. (1996) Function of the upper extremities in hereditary multiple exostoses. J Bone Joint Surg Am. 78(4): 568-573.

• Jacobson LS, et al. (1996) Canine multiple cartilaginous exostoses: unusual manifestations and a review of the literature. J Am Anim Hosp Assoc. 32(1): 45-51.

• Robbins SE, et al. (1996) Hereditary spinal osteochondromas in diaphyseal aclasia. Neuroradiology. 38(1): 59-61.
• Galasso et al. (1996) Growth hormone therapy in two patients with hereditary multiple exostosis. Clin Pediatr (Phila) 35: 657-661.

• Wuyts et al. (1996) Positional cloning of a gene involved in hereditary multiple exostoses. Human Molecular Genetics 5: 1547-1557.

• Stickens et al. (1996) The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes. Nature Genetics 14: 25-32.

• Bartsch et al. (1996) Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11. American Journal of Human Genetics 58: 734-742.

• Potocki and Shaffer (1996) Interstitial deletion of 11(p11.2p12): a newly described contiguous gene deletion syndrome involving the gene for hereditary multiple exostoses (EXT2). American Journal of Human Genetics 62: 319-325.

• Blanton et al. (1996) Hereditary multiple exostoses: confirmation of linkage to chromosomes 8 and 11. American Journal of Medical Genetics 62: 150-159.

• Niikawa et al. (1996) Positional cloning of the putative gene responsible for transient abnormal myelopoiesis and that for multiple cartilaginous exostoses. Rinsho Byori 44: 13-18.

• Goudarzi YM, et al. (1995) Bilateral lesion of the peroneal nerve with lesion of the left-sided median and ulnar nerves in multiple osteocartilaginous exostoses. Chirurg. 66(11): 1158-1161.

• McGaughran JM, et al. (1995) WAGR syndrome and multiple exostoses in a patient with del(11)(p11.2p14.2). J Med Genet. 2(10): 823-824.

• Kobayashi H, et al. (1995) 3D-spiral CT of multiple exostoses. Comput Med Imaging Graph. 19(5): 419-422.

• Taniguchi K. (1995) A practical classification system for multiple cartilaginous exostosis in children. J Pediatr Orthop. 15(5): 585-591.

• Wuyts W, et al. (1995) Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11. Am J Hum Genet. 57(2): 382-387.

• Barros Filho TE, et al. (1995) Hereditary multiple exostoses and cervical ventral protuberance causing dysphagia. A case report. Spine. 20(14): 1640-1642.

• Dendale J, et al. (1995) A rare complication of multiple exostoses: hemothorax. Arch Pediatr. 2(6): 548-550.

• Nawata K, et al. (1995) Knee deformities in multiple hereditary exostoses. A longitudinal radiographic study. Clin Orthop. 313: 194-199.

• Karbowski A, et al. (1995) Multiple cartilagenous exostoses. Orthopade. 24(1): 37-43.

• Castriota-Scanderbeg A, et al. (1995) Spontaneous regression of exostoses: two case reports. Pediatr Radiol. 25(7): 544-548.

• Benhidjeb T, et al. (1995) Occlusion of the popliteal and tibial artery complicating multiple exostoses. Eur J Surg. 161(1): 59-61.

• Bolton P, et al. (1995) Autism, mental retardation, multiple exostoses and short stature in a female with 46,X,t(X;8)(p22.13;q22.1). Psychiatr Genet. 5(2): 51-55.

• Hou et al. (1995) A 4-megabase YAC contig that spans the Langer-Giedion syndrome region on human chromosome 8q24.1: use in refining the location of the trichorhinophalangeal syndrome and multiple exostoses genes (TRPS1 and EXT1). Genomics 29: 87-97.

• Ludecke et al. (1995) Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer-Giedion syndrome. Hum Mol Genet. 4: 31-36.

• Ahn et al. (1995) Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1). Nat Genet 11: 137-143.

• Raskind et al. (1995) Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11. Am J Hum Genet 56: 1132-1139.

• Hecht et al. (1995) Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome II and loss of heterozygosity for EXT-linked markers on chromosomes II and 8. Am J Hum Genet 56: 1125-1131.

• Wicklund et al. (1995) Natural history study of hereditary multiple exostoses. Am J Hum Genet 55: 43-46.

• Richter E. (1994) Rare complications of costal cartilaginous exostoses in childhood. Aktuelle Radiol. 4(6): 318-320.

• Schmale GA, et al. (1994) The natural history of hereditary multiple exostoses. J Bone Joint Surg Am. 76(7): 986-992.

• Venuta A, et al. (1994) The multiple exostoses syndrome. 3 cases in one family. Pediatr Med Chir. 16(4): 403-404.

• O'Brien MF, et al. (1994) Intracanalicular osteochondroma producing spinal cord compression in hereditary multiple exostoses. J Spinal Disord. 7(3): 236-241.

• Rosbotham JL, et al. (1994) An association between psoriasis and hereditary multiple exostoses. A clue for the mapping of a psoriasis susceptibility gene? Br J Dermatol. 130(5): 671-674.

• Le Merrer M, et al. (1994) A gene for hereditary multiple exostoses maps to chromosome 19p. Hum Mol Genet. 3(5): 717-722.

• Kotyla P, et al. (1994) Familial multiple exostoses. Wiad Lek. 47(7-8): 304-306.

• De Stefano N, et al. (1994) Association of myopathy with multiple exostoses and mental retardation: a case report. Brain Dev. 16(2): 136-138.

• Emanuelson I, et al. (1994) Hereditary multiple exostosis with spinal cord compression in a 13-year-old boy. J Neurol Neurosurg Psychiatry. 57(2): 238-239.

• Majumdar AK. (1994) Hereditary multiple exostoses. J Indian Med Assoc. 92(2): 59.

• Wu YQ, et al. (1994) Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11. Hum Mol Genet. 3(1): 167-171.

• Rajewski F. (1994) Use of the Ilizarov method in treatment of forearm deformity due to multiple exostoses. Chir Narzadow Ruchu Ortop Pol. 59(2): 129-132.

• Yoshiura K, et al. (1994) Mapping of the 8q23 translocation breakpoint of t(8;13) observed in a patient with multiple exostoses. Genes Chromosomes Cancer. 9(1): 57-61.

• Dahl MT. (1993) The gradual correction of forearm deformities in multiple hereditary exostoses. Hand Clin. 9(4): 707-718.

• Rodgers WB, et al. (1993) One-bone forearm as a salvage procedure for recalcitrant forearm deformity in hereditary multiple exostoses. J Pediatr Orthop. 13(5): 587-591.

• Castells L, et al. (1993) Case report: haemothorax in hereditary multiple exostosis. Br J Radiol. 66(783): 269-270.

• Recht MP, et al. (1993) Popliteal artery pseudoaneurysm in a patient with hereditary multiple exostoses: MRI and MRA diagnosis. J Comput Assist Tomogr. 17(2): 300-302.

• Eder HG, et al. (1993) Cervical cord compression in hereditary multiple exostoses. J Neurosurg Sci. 37(1): 53-56.

• Black B, et al. (1993) Multiple hereditary exostoses. An epidemiologic study of an isolated community in Manitoba. Clin Orthop. 287: 212-217.

• Burgess RC, et al. (1993) Deformities of the forearm in patients who have multiple cartilaginous exostosis. J Bone Joint Surg Am. 75(1): 13-18.

• Cook et al. (1993) Genetic heterogeneity in families with hereditary multiple exostoses. Am J Hum Genet 53: 71-9.

• Marteaux et al. (1993) Dominant carpotarsal osteochondromatosis. J Med Genet 30: 704-6.

• Del-Rio R, et al. (1992) Multiple exostoses syndrome presenting as nail malalignment and longitudinal dystrophy of fingers. Arch Dermatol. 128(12): 1655-1656.

• Le Merrer M, et al. (1992) The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24). J Med Genet. 29(10): 713-715.

• Hamann G, et al. (1992) Spastic disorder in patients with hereditary multiple exostoses, but without spinal cord compression: a new syndrome? J Med Genet. 29(7): 494-496.

• Glassman SB, et al. (1992) Nuclear medicine case of the day. Hereditary multiple exostoses. AJR Am J Roentgenol. 158(6): 1384.

• Porter G, et al. (1992) Wavy pelvis sign in CT of multiple hereditary osteochondromatosis. J Comput Assist Tomogr. 16(1): 126-128.

• Malghem J, et al. (1992) Benign osteochondromas and exostotic chondrosarcomas: evaluation of cartilage cap thickness by ultrasound. Skeletal Radiol. 21(1): 33-37.

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