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Results for FADD

Publications & Outputs

  1. 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.

    Gregory-Evans, C. Y., Moosajee, M., Hodges, M., Mackay, D. S., Game, L., Vargesson, N., Bloch-Zupan, A., Rüschendorf, F., Santos-Pintos, L., Wackens, G. & Gregory-Evans, K., 2007, In: Human Molecular Genetics. 16, 20, p. 2482-2493 12 p.

    Research output: Contribution to Journal/MagazineJournal articlepeer-review