Orphanet Syndrome BOR
Genomic Landscape of BranchioOtoRenal Syndrome through
Novel likely pathogenic variant in the EYA1 gene causing
A human homologue
of the Drosophila eyes absent gene Nature
Branchio oto renal syndrome
Branchio‐ oto ‐renal syndrome
BOR novel mutations in the
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Branchio
Oto Renal syndrome
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From clinical to molecular diagnosis relevance of diagnostic
Branchiootorenal syndrome BOR novel mutations in the
Branchiootorenal syndrome BOR novel mutations in the
BranchioOtoRenal Syndrome BOR novel mutations in the
Syndrome branchiootorénal
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