Global ETD Search

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Showing 1 to 1 of 1 for “"Phenotype Characterisation"”.

  1. An in vivo study of GTF2IRD1 function and its contribution to the physical features of Williams Beuren Syndrome

    … mouse deletion on neurological and craniofacial phenotypes using direct physiological and cellular analysis methods. A detailed analysis of Gtf2ird1 expression in the inner ear and the skin was conducted. A comprehensive analysis of hearing capacity in Gtf2ird1 knockout mice was carried out by …

    unsw Repository record for An in vivo study of GTF2IRD1 function and its contribution to the physical features of Williams Beuren Syndrome (opens in a new tab)