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4. Genetic control of bone remodeling--insights from a rare disease. Krane SM. N Engl J Med; 2002 Jul 18; 347(3):210-2. PubMed ID: 12124412 [No Abstract] [Full Text] [Related]
9. Determination of a minimal region of loss of heterozygosity on chromosome 18q21.33 in osteosarcoma. Johnson-Pais TL, Nellissery MJ, Ammerman DG, Pathmanathan D, Bhatia P, Buller CL, Leach RJ, Hansen MF. Int J Cancer; 2003 Jun 10; 105(2):285-8. PubMed ID: 12673693 [Abstract] [Full Text] [Related]
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11. Loss of chaotic trabecular structure in OPG-deficient juvenile Paget's disease patients indicates a chaogenic role for OPG in nonlinear pattern formation of trabecular bone. Salmon P. J Bone Miner Res; 2004 May 10; 19(5):695-702. PubMed ID: 15068491 [Abstract] [Full Text] [Related]
12. Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity. Haslam SI, Van Hul W, Morales-Piga A, Balemans W, San-Millan JL, Nakatsuka K, Willems P, Haites NE, Ralston SH. J Bone Miner Res; 1998 Jun 10; 13(6):911-7. PubMed ID: 9626621 [Abstract] [Full Text] [Related]
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18. A probable linkage between familial Paget's disease and the HLA loci. Tilyard MW, Gardner RJ, Milligan L, Cleary TA, Stewart RD. Aust N Z J Med; 1982 Oct 10; 12(5):498-500. PubMed ID: 6295352 [No Abstract] [Full Text] [Related]
19. Deletion of aspartate 182 in OPG causes juvenile Paget's disease by impairing both protein secretion and binding to RANKL. Middleton-Hardie C, Zhu Q, Cundy H, Lin JM, Callon K, Tong PC, Xu J, Grey A, Cornish J, Naot D. J Bone Miner Res; 2006 Mar 10; 21(3):438-45. PubMed ID: 16491292 [Abstract] [Full Text] [Related]
20. Paget's disease from a genetic perspective. Van Hul W. Bone; 1999 May 10; 24(5 Suppl):29S-30S. PubMed ID: 10321923 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]