Fuz mutant mice reveal shared mechanisms between ciliopathies and FGF-related syndromes. [electronic resource]
Producer: 20130903Description: 623-35 p. digitalISSN:- 1878-1551
- Animals
- Bardet-Biedl Syndrome -- genetics
- Cell Movement -- physiology
- Ciliary Motility Disorders -- genetics
- Craniofacial Abnormalities -- genetics
- Cytoskeletal Proteins
- Disease Models, Animal
- Fibroblast Growth Factor 8 -- genetics
- Intracellular Signaling Peptides and Proteins -- genetics
- Kruppel-Like Transcription Factors -- genetics
- Maxilla -- abnormalities
- Mice
- Mice, Mutant Strains
- Neural Crest -- abnormalities
- Orofaciodigital Syndromes -- genetics
- Palate -- abnormalities
- Phenotype
- Zinc Finger Protein GLI1
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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