Bardet–Biedl syndrome
Ciliopathic recessive genetic disorder
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EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome
Retrotransposon insertion as a novel mutational event in Bardet-Biedl syndrome
Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene
Mutations in C8ORF37 cause Bardet Biedl syndrome (BBS21)
Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly
Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome
Leptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndrome
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