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Use of the Cre/lox recombination system to develop a non-lethal knock-in murine model for osteogenesis imperfecta with an alpha1(I) G349C substitution. Variability in phenotype in BrtlIV mice |
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| Authors: | Forlino A Porter F D Lee E J Westphal H Marini J C |
| Institution: | Heritable Disorders Branch, NICHD, National Institutes of Health, Bethesda, Maryland 20892, USA. |
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