Showing results 2 to 3 of 3
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Title | Author(s) | Issue Date | |
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Marfan syndrome: Absence of type I or III collagen structural defects in 25 patients Journal:Journal of Inherited Metabolic Disease | 1990 | ||
Type X collagen multimer assembly in vitro is prevented by a Gly618 to Val mutation in the α1(X) NC1 domain resulting in Schmid metaphyseal chondrodysplasia Journal:Journal of Biological Chemistry | 1995 |