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APA Citation
Yamada, M., Funato, M., Kondo, G., Suzuki, H., Uehara, T., Takenouchi, T., Sakamoto, Y., & Kosaki, K. (2021). noonan syndrome‐like phenotype in a patient with heterozygous ERF truncating variant. Congenital anomalies, 61, 226–230. http://access.bl.uk/ark:/81055/vdc_100145639932.0x000032