• A Case of Laurence Moon Bardet Biedl Syndrome
• Bardet-Biedl syndrome associated with novel compound heterozygous variants in BBS12 gene
• Bardet-Biedl Syndrome Overview
• Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome
• Caregiver burden in Bardet-Biedl syndrome: findings from the CARE-BBS study
• Congenital Hepatic Fibrosis Overview ─ RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY
• Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees
• Exome sequencing in a Romanian Bardet-Biedl syndrome cohort revealed an overabundance of causal BBS12 variants
• Genetic Obesity Disorders: Body Mass Index Trajectories and Age of Onset of Obesity Compared with Children with Obesity from the General Population
• Laparoscopic Sleeve Gastrectomy in a Morbidly Obese Pediatric Patient With Bardet-Biedl Syndrome
• Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet-Biedl and Usher Syndromes
• Next-Generation Sequencing of a Large Gene Panel for Outcome Prediction of Bariatric Surgery in Patients with Severe Obesity
• Nonsyndromic Retinitis Pigmentosa Overview
• Organization, functions, and mechanisms of the BBSome in development, ciliopathies, and beyond
• Outcomes in children of women with type 2 diabetes exposed to metformin versus placebo during pregnancy (MiTy Kids): a 24-month follow-up of the MiTy randomised controlled trial
• Phenotype and genotype spectra of a Chinese cohort with nephronophthisis-related ciliopathy
• Proteomic and Transcriptomic Landscapes of Alström and Bardet-Biedl Syndromes
• Quality of life improvements following one year of setmelanotide in children and adult patients with Bardet-Biedl syndrome: phase 3 trial results