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8q22.2 Deletion

11
Aug

8q22.2 Deletion

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Deng et al. “Heterozygous loss of OSR2 can cause radioulnar synostosis with ancillary skeletal manifestations”. “Genetics in Medicine” 2026, v. 28(3), 101664. Congenital radioulnar synostosis (RUS) is defined by bony fusion of the proximal radius and ulna bones. Genetic causes have previously been identified such as pathogenic variants in SMAD6...
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