StructureFunction
Analyses of the Human
SIX1EYA2 Complex
Clinically diverse phenotypes and genotypes of patients with
Branchio oto renal syndrome
Orphanet BOR syndrome
Branchiootorenal syndrome identification of novel PubMed
BranchioOtoRenal Syndrome BOR novel mutations in the
Branchiootorenal Spectrum Disorder GeneReviews® NCBI
Branchiootorenal syndrome BOR novel mutations in the
Genomic Landscape of BranchioOtoRenal Syndrome through
PDF
Molecular Genetic Causes and Clinical ResearchGate
Branchiootorenal syndrome PubMed
A human homologue of the Drosophila eyes absent gene Nature
Otobor Spray Auric 50Ml
Branchio‐ oto ‐renal syndrome BOR novel mutations in the
A human homologue of the Drosophila eyes absent gene
Orphanet Syndrome BOR
From clinical to molecular diagnosis relevance
of diagnostic