(Q46296275)

21 December 2017

http://europepmc.org/abstract/MED/8335019

title

Defective collagen fibril formation and mineralization in osteogenesis imperfecta with congenital joint contractures (Bruck syndrome). (English)

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

main subject

osteogenesis imperfecta

0 references

author name string

R E Brenner

1

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

U Vetter

2

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

H Stöss

3

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

P K Müller

4

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

W M Teller

5

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

publication date

1 June 1993

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

published in

European Journal of Pediatrics

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

volume

152

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

issue

6

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

page(s)

505-508

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

cites work

A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01955060

Brittle bones--fragile molecules: disorders of collagen gene structure and expression

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01955060

Changes in apatite crystal size in bones of patients with osteogenesis imperfecta

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/8335019

12 December 2020

Osteogenesis imperfecta: A clinical study of the first ten years of life

1 reference

https://pubmed.ncbi.nlm.nih.gov/8335019

12 December 2020

OSTEOGENESIS IMPERFECTA WITH ARTHROGRYPOSIS MULTIPLEX CONGENITA

1 reference

https://pubmed.ncbi.nlm.nih.gov/8335019

12 December 2020

Two bovine models of osteogenesis imperfecta exhibit decreased apatite crystal size

1 reference

https://pubmed.ncbi.nlm.nih.gov/8335019

12 December 2020

Osteogenesis imperfecta with congenital joint contractures (Bruck syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8335019

12 December 2020

Structural changes of collagen fibrils in skeletal dysplasias. Ultrastructural findings in the iliac crest

1 reference

https://pubmed.ncbi.nlm.nih.gov/8335019

12 December 2020

Genetic heterogeneity in osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/8335019

12 December 2020

The estimation of two collagens from human dermis by interrupted gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8335019

12 December 2020

Osteogenesis imperfecta: insufficient collagen synthesis in early childhood as evidenced by analysis of compact bone and fibroblast cultures

1 reference

https://pubmed.ncbi.nlm.nih.gov/8335019

12 December 2020

Type I procollagen: the gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissue.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8335019

12 December 2020

Identifiers

DOI

10.1007/BF01955060

1 reference

21 December 2017

http://europepmc.org/abstract/MED/8335019

1 reference

21 December 2017