AR 07713/AR/NIAMS NIH HHS/United States[Grants and Funding] - Search Results

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Osteogenesis imperfecta: the molecular basis of clinical heterogeneity.

Byers PH, Bonadio JF, Cohn DH, Starman BJ, Wenstrup RJ, Willing MC. Byers PH, et al. Ann N Y Acad Sci. 1988;543:117-28. doi: 10.1111/j.1749-6632.1988.tb55324.x. Ann N Y Acad Sci. 1988. PMID: 3063158 Free article. Review. No abstract available.

Osteogenesis imperfecta and other inherited disorders of the structure and synthesis of type I collagen: models for the analysis of mutations that result in inherited chondrodysplasias.

Cohn DH, Byers PH. Cohn DH, et al. Pathol Immunopathol Res. 1988;7(1-2):132-8. doi: 10.1159/000157108. Pathol Immunopathol Res. 1988. PMID: 3065765 Review. No abstract available.

General strategies for isolating the genes encoding type I collagen and for characterizing mutations which produce osteogenesis imperfecta.

Cohn DH, Wenstrup RJ, Willing MC, Bonadio JF, Byers PH. Cohn DH, et al. Ann N Y Acad Sci. 1988;543:129-35. doi: 10.1111/j.1749-6632.1988.tb55325.x. Ann N Y Acad Sci. 1988. PMID: 3063159 Free article. Review. No abstract available.

A novel mutation causes a perinatal lethal form of osteogenesis imperfecta. An insertion in one alpha 1(I) collagen allele (COL1A1).

Byers PH, Starman BJ, Cohn DH, Horwitz AL. Byers PH, et al. J Biol Chem. 1988 Jun 5;263(16):7855-61. J Biol Chem. 1988. PMID: 3372508 Free article.

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