TY  - GEN
AU  - Tabler,Jacqueline M
AU  - Barrell,William B
AU  - Szabo-Rogers,Heather L
AU  - Healy,Christopher
AU  - Yeung,Yvonne
AU  - Perdiguero,Elisa Gomez
AU  - Schulz,Christian
AU  - Yannakoudakis,Basil Z
AU  - Mesbahi,Aida
AU  - Wlodarczyk,Bogdan
AU  - Geissmann,Frederic
AU  - Finnell,Richard H
AU  - Wallingford,John B
AU  - Liu,Karen J
TI  - Fuz mutant mice reveal shared mechanisms between ciliopathies and FGF-related syndromes
SN  - 1878-1551
PY  - 2013///0903
KW  - Animals
KW  - Bardet-Biedl Syndrome
KW  - genetics
KW  - Cell Movement
KW  - physiology
KW  - Ciliary Motility Disorders
KW  - Craniofacial Abnormalities
KW  - Cytoskeletal Proteins
KW  - Disease Models, Animal
KW  - Fibroblast Growth Factor 8
KW  - Intracellular Signaling Peptides and Proteins
KW  - Kruppel-Like Transcription Factors
KW  - Maxilla
KW  - abnormalities
KW  - Mice
KW  - Mice, Mutant Strains
KW  - Neural Crest
KW  - Orofaciodigital Syndromes
KW  - Palate
KW  - Phenotype
KW  - Zinc Finger Protein GLI1
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.devcel.2013.05.021
ER  -