Genetic aspects of familial osteoarthritis.
- 1 December 1994
- journal article
- review article
- Published by BMJ in Annals Of The Rheumatic Diseases
- Vol. 53 (12), 789-797
- https://doi.org/10.1136/ard.53.12.789
Abstract
No abstract availableThis publication has 44 references indexed in Scilit:
- Identification of a mutation in type X collagen in a family with Schmid metaphyseal chondrodysplasiaHuman Molecular Genetics, 1994
- A type X collagen mutation causes Schmid metaphyseal chondrodysplasiaNature Genetics, 1993
- Calcium pyrophosphate dihydrate crystal deposition in synovium. relationship to collagen fibers and chondrometaplasiaArthritis & Rheumatism, 1993
- Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defectNature Genetics, 1993
- Genetic Linkage of a Polymorphism in the Type II Procollagen Gene (COL2A1) to Primary Osteoarthritis Associated with Mild ChondrodysplasiaNew England Journal of Medicine, 1990
- PREDISPOSITION TO FAMILIAL OSTEOARTHROSIS LINKED TO TYPE II COLLAGEN GENEThe Lancet, 1989
- Diagnosis of Genetic Disorders at the DNA LevelNew England Journal of Medicine, 1989
- Structure of the major block of alphoid satellite DNA on the human Y chromosomeJournal of Molecular Biology, 1987
- HLA and Heberden's nodes in Mexican MestizosClinical Rheumatology, 1985
- Morphological study of articular cartilage in pyrophosphate arthropathy. (Chondrocalcinosis articularis or calcium pyrophosphate dihydrate crystal deposition diseases).Annals Of The Rheumatic Diseases, 1972