Cite

    Oliver, G. R., Blackburn, P. R., Ellingson, M. S., Conboy, E., Pinto e Vairo, F., Webley, M., Thorland, E., Ferber, M., Van Hul, E., van der Werf, I. M., Wuyts, W., Babovic‐Vuksanovic, D., & Klee, E. W. (2019). rNA‐Seq detects a SAMD12‐EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromas. Molecular genetics & genomic medicine, 7(3), n/a. http://access.bl.uk/ark:/81055/vdc_100117760848.0x000005