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Browsing by Author "Sadler, Françoise"

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ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders : novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants

Weisschuh, Nicole; Kohl, Susanne; Wissinger, Bernd; Sadler, Françoise (2019)
Impact of OCT scan-patterns in identifying morphological features of lamellar macular holes and macular pseudoholes

Konrad, Eva-Maria; Gelisken, Faik; Neubauer, Jonas; Sadler, Françoise (2022)

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