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APA Citation
Accogli, A., Traverso, M., Madia, F., Bellini, T., Vari, M. S., Pinto, F., & Capra, V. (2017). a novel Xp22.13 microdeletion in Nance‐Horan syndrome. Birth defects research, 109(11), 866–868. http://access.bl.uk/ark:/81055/vdc_100058803233.0x000013