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2. Type II collagen defect in two sibs with the Goldblatt syndrome, a chondrodysplasia with dentinogenesis imperfecta, and joint laxity. Bonaventure J, Stanescu R, Stanescu V, Allain JC, Muriel MP, Ginisty D, Maroteaux P. Am J Med Genet; 1992 Dec 01; 44(6):738-53. PubMed ID: 1481841 [Abstract] [Full Text] [Related]
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5. In vitro expression of osteoblastic markers in cells isolated from normal fetal and postnatal human bone and from bone of patients with osteogenesis imperfecta. Mörike M, Schulz M, Brenner RE, Bushart GB, Teller WM, Vetter U. J Cell Physiol; 1993 Dec 01; 157(3):439-44. PubMed ID: 8253854 [Abstract] [Full Text] [Related]
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19. Achondrogenesis type IB (Fraccaro): study of collagen in the tissue and in chondrocytes cultured in agarose. Freisinger P, Stanescu V, Jacob B, Cohen-Solal L, Maroteaux P, Bonaventure J. Am J Med Genet; 1994 Feb 15; 49(4):439-46. PubMed ID: 8160740 [Abstract] [Full Text] [Related]