Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet-Biedl syndrome.

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Mutations in C8ORF37 cause Bardet Biedl syndrome (BBS21)Clinical prediction model to identify vulnerable patients in ambulatory surgery: towards optimal medical decision-making.Genetic analysis of very obese children with autism spectrum disorder.

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Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet-Biedl syndrome.

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Exploration of the cognitive, ...... ed with Bardet-Biedl syndrome.

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P2860

Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes

Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin.

Ciliopathy is differentially distributed in the brain of a Bardet-Biedl syndrome mouse model

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.

The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome.

Cilia in the nervous system: linking cilia function and neurodevelopmental disorders.

Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactyly.

The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland. Clinical, genetic and epidemiological studies.

Behavioural phenotype of Bardet-Biedl syndrome.

Screening of 336 single-nucleotide polymorphisms in 85 obesity-related genes revealed McKusick-Kaufman syndrome gene variants are associated with metabolic syndrome.

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Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet-Biedl syndrome.

about

P2860

P2860

Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet-Biedl syndrome.

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