Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different from FGFR, TWIST, and MSX2. [electronic resource]
Producer: 20030407Description: 200-6 p. digitalISSN:- 0148-7299
- Adult
- Child
- Child, Preschool
- Craniosynostoses -- complications
- DNA -- chemistry
- DNA Mutational Analysis
- DNA-Binding Proteins -- genetics
- Exons -- genetics
- Eye Diseases -- complications
- Family Health
- Genetic Predisposition to Disease -- genetics
- Homeodomain Proteins
- Humans
- Limb Deformities, Congenital -- complications
- Male
- Mutation
- Nuclear Proteins
- Protein-Tyrosine Kinases
- Receptor Protein-Tyrosine Kinases -- genetics
- Receptor, Fibroblast Growth Factor, Type 1
- Receptor, Fibroblast Growth Factor, Type 2
- Receptor, Fibroblast Growth Factor, Type 3
- Receptors, Fibroblast Growth Factor -- genetics
- Transcription Factors -- genetics
- Twist-Related Protein 1
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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