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

Cheryl Y. Gregory-Evans, Mariya Moosajee, Matthew D. Hodges, Donna S. Mackay, Laurence Game, Neil Vargesson, Agnès Bloch-Zupan, Franz Rüschendorf, Lourdes Santos-Pinto, Georges Wackens, Kevin Gregory-Evans

Research output: Contribution to journal › Article › peer-review

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Medicine & Life Sciences