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antley-bixler syndrome with genital anomalies and disordered steroidogenesis
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Impact on CYP19A1 activity by mutations in NADPH cytochrome P450 oxidoreductase
Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes
Radio-ulnar synostosis in Williams syndrome. A frequently associated anomaly
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