idw – Informationsdienst Wissenschaft
Nachrichten, Termine, Experten
Nachrichten, Termine, Experten
Ein typischer Chromosomensatz eines sSMC-Trägers: in diesem Fall eines klinisch auffälligen Kindes nach Bänderungszytogenetik - ist in der linken Bildhälfte zu sehen. Das Markerchromosom ist rot umrandet. Das sSMC konnte erst nach Einsatz einer Fluoreszenz-in-situ-Hybridisierung - u. a. mittels einer Vielfarbenbänderungs-Sonde für Chromosom 18 (rechte Bildhälfte) - charakterisiert werden als zusätzliches Isochromosom 18p: typisch für das i(18p)-Syndrom.
Foto: Liehr/FSU
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