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SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma
Imperial College London; Universite Louis Pasteur; Max Delbrück Center for Molecular Medicine; Universidade de São Paulo (USP); Free University of Brussels
Gregory-Evans, Cheryl Y.; Moosajee, Mariya; Hodges, Matthew D.; Mackay, Donna S.; Game, Laurence; Vargesson, Neil; Bloch-Zupan, Agnès; Rüschendorf, Franz; Santos-Pinto, Lourdes; Wackens, Georges; Gregory-Evans, Kevin
29-Abr-2022
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