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. 2017 May 4;11(2):299–307. doi: 10.3897/CompCytogen.11(2).11942

Figure 1.

Figure 1.

Karyotypes of Chaetodipterus faber (A), Lutjanus synagris (B), and Rypticus randalli (C) with 2n=48 acrocentric chromosomes after conventional Giemsa-staining (top), C-banding (center) and double FISH with 18S (green signals) and 5S (magenta signals) rDNA probes (bottom). In boxes, the pairs bearing nucleolus organizer regions after silver nitrate staining (Ag-NORs).