Prenatal Diagnosis and Prevention of Inherited Abnormalities of Collagen
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Publisher
Springer Netherlands
Link
http://link.springer.com/content/pdf/10.1007/978-94-009-1069-0_12.pdf
Reference107 articles.
1. Barsh, G. S. and Byers, P. H. Abnormal secretion of type I procollagen in a variety of osteogenesis imperfecta. Proc. Natl. Acad. Sci. USA 8 (1981) 5142–5146
2. Barsh, G. S., David, K. and Byers, P. H. Type 1 osteogenesis imperfecta; a non-functional allele for pro al(I) chains of type I procollagen. Proc. Natl. Acad. Sci. USA 79 (1982) 3838–3842
3. Barsh, G. S., Roush, C., Bonadio, J. et sl. Intron mediated recombination may cause a deletion in an Ø1(I) chains of type I Procollagen. Proc. Natl. Acad. Sci. USA 79 (1982) 3838-3842.
4. Bateman, J. F., Chan, D., Walker, I. D. et al Lethal perinatal osteogenesis imperfecta due to a substitution of arginine for glycine at residue 391 of the al(I) chain of type I collagen. J. Biol. Chem. 262 (1987) 7021–7027
5. Bateman, J. F., Lamande, S. R., Dahl, H-H. M. et al Substitution of arginine for glycine 664 in the collagen al chain in lethal perinatal OI. J. Biol. Chem. 263 (1988) 11625–11630
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