Showing results 1 to 3 of 3
| Title | Author(s) | Issue Date | |
|---|---|---|---|
| 1996 | |||
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 |