Deficiencies that modify the ey>hid-p35-induced AiP phenotype as suppressors or enhancers.
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The indicated chromosomal location is the smallest overlap of overlapping deficiencies. Df(2L)TW137 is marked with a “?” because other overlapping deficiencies do not suppress AiP (see Suppl. Table S1) indicating that the Df(2L)TW137 chromosome carries a suppressor mutation independent of the deficiency.
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2015-12-02
