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45. [Unusual development of vertebral exostosis in a child]. BOLLETTI M Acta Paediatr Lat; 1951; 4(6):458-72. PubMed ID: 14902453 [No Abstract] [Full Text] [Related]
46. [Study of Bessel-Hagen osteogenic disease]. PASTON P Praxis; 1959 Mar; 48(12):291-3. PubMed ID: 13645401 [No Abstract] [Full Text] [Related]
47. [Chondrogenic exostosis; a case of systemic type]. AGUIRRE JA; ORLANDO JC Med Panam; 1958 Nov; 11(9-10):401-7. PubMed ID: 13632298 [No Abstract] [Full Text] [Related]
49. [Exostotic disease and pulmonary hypoplasia]. DUROUX A J Fr Med Chir Thorac; 1958; 12(4):448-50. PubMed ID: 13598852 [No Abstract] [Full Text] [Related]
50. [Iconography of a case of exostotic disease with chondromatous inclusions; radiographic enlargements]. LAYANI F; FISCHGOLD H Presse Med (1893); 1953 Dec; 61(82):1768-72. PubMed ID: 13134088 [No Abstract] [Full Text] [Related]
51. [Exostotic disease and its classification among congenital chondrodysplastic bone diseases; case reports]. SVILOKOS N; VERDURA G; SERAFINI L Minerva Pediatr; 1959 Mar; 11(11):296-302. PubMed ID: 13656827 [No Abstract] [Full Text] [Related]
52. [Multiple cartilaginous and hereditary exostoses]. PFANDLER U Schweiz Med Wochenschr; 1948 Mar; 78(10):230-2. PubMed ID: 18916666 [No Abstract] [Full Text] [Related]
53. Pseudoaneurysm associated with multiple osteochondromatosis. Bursztyn M; Stracher M; Sanchez JI; Ramenofsky M; Kirwin J; Spero C J Pediatr Surg; 2005 Jul; 40(7):1201-3. PubMed ID: 16034773 [TBL] [Abstract][Full Text] [Related]
54. Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis). Faiyaz-Ul-Haque M; Ahmad W; Zaidi SH; Hussain S; Haque S; Ahmad M; Cohn DH; Tsui LC Clin Genet; 2004 Aug; 66(2):144-51. PubMed ID: 15253765 [TBL] [Abstract][Full Text] [Related]
56. Intra-articular osteochondroma of the knee joint in a patient with hereditary multiple osteochondromatosis. Matsumoto Y; Matsuda S; Matono K; Oda Y; Tsuneyoshi M; Iwamoto Y Fukuoka Igaku Zasshi; 2007 Dec; 98(12):425-30. PubMed ID: 18260368 [TBL] [Abstract][Full Text] [Related]
57. Two-color multiplex ligation-dependent probe amplification: detecting genomic rearrangements in hereditary multiple exostoses. White SJ; Vink GR; Kriek M; Wuyts W; Schouten J; Bakker B; Breuning MH; den Dunnen JT Hum Mutat; 2004 Jul; 24(1):86-92. PubMed ID: 15221792 [TBL] [Abstract][Full Text] [Related]