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Article

[Bardet-Biedl syndrome: a unique family for a major gene (BBS10)].

Medecine sciences : M/S - 1 Nov 2006

Dollfus Hélène, Muller Jean, Stoetzel Corinne, Laurier Virginie, Bonneau Dominique, Mégarbané André, Poch Olivier, Mandel Jean-Louis

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Identifiers

PMID: 17101080
DOI: 10.1051/medsci/20062211901

Genes

BBS10

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Bardet-Biedl syndrome: a unique family for a major gene (BBS10)].PMID 17101080Read ↗

The major gene for Bardet-Biedl syndrome is BBS1.Semantic proximity Read ↗

Novel mutations in BBS5 highlight the importance of this gene in non-Caucasian Bardet-Biedl syndrome patients.Semantic proximity Read ↗

Two sibs with Bardet-Biedl syndrome due to mutations in BBS12: no clues for modulation by a third mutation in BBS10.Semantic proximity Read ↗

[Bardet-Biedl syndrome. Insight into this rare inherited syndrome can lead to new knowledge of molecular mechanisms].Semantic proximity Read ↗

Genetics of human Bardet-Biedl syndrome, an updates.Semantic proximity Read ↗

Expanding the phenotype of Bardet-Biedl syndrome: Newly diagnosed sibling cases.Semantic proximity Read ↗

Whole Exome Sequencing in 11 Iranian Patients Expands the Mutational and Clinical Spectrum of Bardet- Biedl SyndromeSemantic proximity Read ↗

[Biemond syndrome].Semantic proximity Read ↗

A novel homozygous 10 nucleotide deletion in BBS10 causes Bardet-Biedl syndrome in a Pakistani family.Semantic proximity Read ↗

Identification of compound heterozygous mutations in the BBS7 gene in a Korean family with Bardet-Biedl syndrome.Semantic proximity Read ↗

Molecular analysis of Bardet-Biedl syndrome families: report of 21 novel mutations in 10 genes.Semantic proximity Read ↗

Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).Semantic proximity Read ↗

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