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Items: 10

1.

Additional mutations of type X collagen confirm COL10A1 as the Schmid metaphyseal chondrodysplasia locus.

McIntosh I, Abbott MH, Warman ML, Olsen BR, Francomano CA.

Hum Mol Genet. 1994 Feb;3(2):303-7.

PMID:
8004099
2.

Mutations in collagen genes resulting in metaphyseal and epiphyseal dysplasias.

Olsen BR.

Bone. 1995 Aug;17(2 Suppl):45S-49S. Review.

PMID:
8579897
3.

Heritable diseases of cartilage caused by mutations in collagen genes.

Williams CJ, Jimenez SA.

J Rheumatol Suppl. 1995 Feb;43:28-33. Review.

PMID:
7752129
4.

From collagen chemistry towards cell therapy - a personal journey.

Grant ME.

Int J Exp Pathol. 2007 Aug;88(4):203-14. Review.

5.

Metaphyseal chondrodysplasia, Schmid type. Clinical and radiographic delineation with a review of the literature.

Lachman RS, Rimoin DL, Spranger J.

Pediatr Radiol. 1988;18(2):93-102. Review.

PMID:
3281118
6.

[Collagen genes and skeletal disorders].

Kimura T, Tsumaki N, Matsui Y.

Ryumachi. 1995 Jun;35(3):600-8. Review. Japanese. No abstract available.

PMID:
7570217
7.

Mapping collagen gene mutations.

Sykes B.

Ann N Y Acad Sci. 1990;580:385-9. Review. No abstract available.

PMID:
2186695
8.

Clinical--molecular correlations in the skeletal dysplasias.

Rimoin DL, Cohn DH, Eyre D.

Pediatr Radiol. 1994;24(6):425-6. Review. No abstract available.

PMID:
7700719
9.

The collagen superfamily--diverse structures and assemblies.

Hulmes DJ.

Essays Biochem. 1992;27:49-67. Review. No abstract available.

PMID:
1425603
10.

[Diversified expression and function of minor fibrillar collagen].

Yoshioka H.

Seikagaku. 1999 Jun;71(6):432-8. Review. Japanese. No abstract available.

PMID:
10432836

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