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APA Citation
Borck, G., Redon, R., Sanlaville, D., Rio, M., Prieur, M., Lyonnet, S., Vekemans, M., Carter, N. P., Munnich, A., Colleaux, L., & Cormier-Daire, V. (2004). nIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome. Journal of medical genetics, 41(12), e128. http://access.bl.uk/ark:/81055/vdc_100137792990.0x00003c