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Developmental Cell|December 17, 2008
How to shape cells and influence polarized protein traffickingAnna Diaz-Font, Philip L BealesFrontiers in Pediatrics|March 1, 2018
Managing Bardet-Biedl Syndrome-Now and in the FutureElizabeth Forsythe, Joanna Kenny, Chiara Bacchelli, et al.Human Molecular Genetics|January 14, 2011
An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of ciliaSuzanne Rix, Amelie Calmont, Peter J Scambler, et al.Chest|October 16, 2014
Bardet Biedl syndrome: motile ciliary phenotypeAmelia Shoemark, Mellisa Dixon, Philip L Beales, et al.Journal of Visualized Experiments : Jove|March 6, 2015
Evaluation of zebrafish kidney function using a fluorescent clearance assaySonia Christou-Savina, Philip L Beales, Daniel P S OsbornHuman Mutation|July 23, 2003
Evaluation of multiplex capillary heteroduplex analysis: a rapid and sensitive mutation screening techniqueBethan E Hoskins, Anita Thorn, Peter J Scambler, et al.Nature Genetics|May 1, 2007
IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophyPhilip L Beales, Elizabeth Bland, Jonathan L Tobin, et al.Ophthalmic Genetics|September 4, 2008
Bardet-biedl syndrome: an atypical phenotype in brothers with a proven BBS1 mutationPaul S Cannon, Jill Clayton-Smith, Philip L Beales, et al.Frontiers in Endocrinology|July 17, 2026
Hyperphagia severity is underestimated in adults with Bardet-Biedl syndrome - a mixed-method cross-sectional study in the United KingdomJean Mossman, Sarah Flack, Elise Gamertsfelder, et al.Proceedings of the National Academy of Sciences of the United States of America|April 30, 2008
Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndromeJonathan L Tobin, Matt Di Franco, Erica Eichers, et al.Pageof 11