## Communicated by Richard G.H. Cotton Mutations in the type I collagen genes COL1A1 and COL1A2 are responsible for the dominantly inherited connective tissue disorder osteogenesis imperfecta (OI). The severity of OI is diverse, ranging from perinatal lethality to a very mild phenotype that is cha
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Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families
β Scribed by Mottes, Monica ;Sangalli, Antonella ;Pignatti, Pier Franco
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 707 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0148-7299
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