Osteogenesis Imperfecta: A Review with Clinical Examples.
- Published in:
- Molecular Syndromology, 2011, v. 2, n. 1, p. 1, doi. 10.1159/000332228
- By:
- Publication type:
- Article
Works matching IS 16618769 AND DT 2011 AND VI 2 AND IP 1
Results: 6
1
2
Dysspondyloenchondromatosis: Another COL2A1-Related Skeletal Dysplasia?
- Published in:
- Molecular Syndromology, 2011, v. 2, n. 1, p. 21, doi. 10.1159/000333098
- By:
- Publication type:
- Article
3
Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies.
- Published in:
- Molecular Syndromology, 2011, v. 2, n. 1, p. 27, doi. 10.1159/000334317
- By:
- Publication type:
- Article
4
22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review.
- Published in:
- Molecular Syndromology, 2011, v. 2, n. 1, p. 35, doi. 10.1159/000334262
- By:
- Publication type:
- Article
5
Severe Developmental Delay in a Patient with 7p21.1-p14.3 Microdeletion Spanning the TWIST Gene and the HOXA Gene Cluster.
- Published in:
- Molecular Syndromology, 2011, v. 2, n. 1, p. 45, doi. 10.1159/000334313
- By:
- Publication type:
- Article
6
Targeting Mitochondria by Olesoxime or Complement 1q Binding Protein as a Novel Management for Autism: A Hypothesis.
- Published in:
- Molecular Syndromology, 2011, v. 2, n. 1, p. 50, doi. 10.1159/000332202
- By:
- Publication type:
- Article