✦ LIBER ✦
The molecular defect in a family with mild atypical osteogenesis imperfecta and extreme joint hypermobility: Exon skipping caused by an 11-bp deletion from an intron in one COL1A2 allele
✍ Scribed by A. C. Nicholls; J. Oliver; D. V. Renouf; D. A. Heath; F. M. Pope
- Publisher
- Springer
- Year
- 1992
- Tongue
- English
- Weight
- 1009 KB
- Volume
- 88
- Category
- Article
- ISSN
- 0340-6717
No coin nor oath required. For personal study only.