Format
Items per page
Sort by

Send to:

Choose Destination

Results: 9

1.

Genotype-phenotype study in type V osteogenesis imperfecta.

Balasubramanian M, Parker MJ, Dalton A, Giunta C, Lindert U, Peres LC, Wagner BE, Arundel P, Offiah A, Bishop NJ.

Clin Dysmorphol. 2013 Jul;22(3):93-101. doi: 10.1097/MCD.0b013e32836032f0.

PMID:
23612438
2.

Lethal osteogenesis imperfecta-like condition with cutis laxa and arterial tortuosity in MZ twins due to a homozygous fibulin-4 mutation.

Erickson LK, Opitz JM, Zhou H.

Pediatr Dev Pathol. 2012 Mar-Apr;15(2):137-41. doi: 10.2350/11-03-1010-CR.1. Epub 2011 Nov 9.

PMID:
22070778
3.

Lysyl hydroxylation in collagens from hyperplastic callus and embryonic bones.

Lehmann HW, Bodo M, Frohn C, Nerlich A, Rimek D, Notbohm H, Müller PK.

Biochem J. 1992 Mar 1;282 ( Pt 2):313-8.

4.

A critical crosslink region in human-bone-derived collagen type I. Specific cleavage site at residue Leu95.

Bätge B, Notbohm H, Diebold J, Lehmann H, Bodo M, Deutzmann R, Müller PK.

Eur J Biochem. 1990 Aug 28;192(1):153-9.

6.

Biochemical analysis of callus tissue in osteogenesis imperfecta type IV. Evidence for transient overmodification in collagen types I and III.

Brenner RE, Vetter U, Nerlich A, Wörsdorfer O, Teller WM, Müller PK.

J Clin Invest. 1989 Sep;84(3):915-21.

7.
8.
9.
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk