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APA Citation
Hague, J., Delon, I., Brugger, K., Martin, H., Abbs, S., & Park, S. (2016). molecularly proven mosaicism in phenotypically normal parent of a girl with Freeman–Sheldon Syndrome caused by a pathogenic MYH3 mutation. American journal of medical genetics, 170(6), 1608–1612. http://access.bl.uk/ark:/81055/vdc_100032419490.0x00002f