Journal article

Clinical phenotypes associated with type II collagen mutations

Peter Kannu, John Bateman, Ravi Savarirayan

Journal of Paediatrics and Child Health | WILEY-BLACKWELL | Published : 2012

DOI: 10.1111/j.1440-1754.2010.01979.x

Grants

Funding Acknowledgements

Grant supporters: National Health and Medical Research Council (NHMRC) Australia.

Citation metrics

42Web of Science
50Scopus

Keywords

Child
Bilateral Perthes Disease
Life Sciences & Biomedicine
Stickler Syndrome
Collagen Diseases
Humans
Calve-Perthes-Disease
Multiple Epiphyseal Dysplasia (med)
Mutation
Collagen Type Ii
Musculoskeletal Abnormalities
Child, Preschool
Epiphyseal Dysplasia
Phenotype
Molecular-Genetics
Stickler-Syndrome
Infant, Newborn
Col2a1
Chondrodysplasias
Femoral-Head
Osteochondrodysplasias
C-Propeptide
Pediatrics
Skeletal Dysplasia
Spectrum
Legg-Calve-Perthes Disease
Osteoarthritis
Col2a1 Gene
Science & Technology