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Yamada, M. et al. (2021). Noonan syndrome‐like phenotype in a patient with heterozygous ERF truncating variant. Congenital anomalies. pp. 226-230. [Online].
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Yamada, M. et al. (2021). Noonan syndrome‐like phenotype in a patient with heterozygous ERF truncating variant. Congenital anomalies. pp. 226-230. [Online].