Conditional inactivation ofSox9: A mouse model for campomelic dysplasia
Author:
Publisher
Wiley
Subject
Cell Biology,Endocrinology,Genetics
Reference15 articles.
1. Sox9 is required for cartilage formation
2. Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization
3. Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
4. DNA-binding properties of the HMG domain of the lymphoid-specific transcriptional regulator LEF-1.
5. The campomelic syndrome: Review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971
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