Tabler, Jacqueline M <br/><br/>
Fuz mutant mice reveal shared mechanisms between ciliopathies and FGF-related syndromes.  [electronic resource] 

 -  Developmental cell  Jun 2013 
 - 623-35 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1878-1551 
<br/><br/><label>Standard No.: </label>10.1016/j.devcel.2013.05.021  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Bardet-Biedl Syndrome--genetics<br/>Cell Movement--physiology<br/>Ciliary Motility Disorders--genetics<br/>Craniofacial Abnormalities--genetics<br/>Cytoskeletal Proteins<br/>Disease Models, Animal<br/>Fibroblast Growth Factor 8--genetics<br/>Intracellular Signaling Peptides and Proteins--genetics<br/>Kruppel-Like Transcription Factors--genetics<br/>Maxilla--abnormalities<br/>Mice<br/>Mice, Mutant Strains<br/>Neural Crest--abnormalities<br/>Orofaciodigital Syndromes--genetics<br/>Palate--abnormalities<br/>Phenotype<br/>Zinc Finger Protein GLI1