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Congenital dyserythropoiesis anemia type Ia with a novel CDAN1 mutation diagnosed by whole exome sequencing.
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Supplement: MGG3-8-e1220-s001.xlsx › ___1
Molecular profiling of driver events in metastatic uveal melanoma.
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Supplement: 41467_2020_15606_MOESM4_ESM.xlsx › All_variants
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