Associated Papers
Sequence variants in different genes underlying Bardet-Biedl syndrome in four consanguineous families.
Ali A et al.
Molecular Biology Reports, 2023
Mutation profile of Bardet-Biedl syndrome patients from India: Implicative role of multiallelic rare variants and oligogenic inheritance pattern.
Gnanasekaran H et al.
Clinical Genetics, 2023
Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome.
Nawaz H et al.
Genes, 2023
A data set of variants derived from 1455 clinical and research exomes is efficient in variant prioritization for early-onset monogenic disorders in Indians.
Kausthubham N et al.
Human Mutation, 2021
Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families.
Ullah A et al.
Molecular Vision, 2017
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