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APA Citation
Braunholz, D., Obieglo, C., Parenti, I., Pozojevic, J., Eckhold, J., Reiz, B., Brænne, I., Wendt, K. S., Watrin, E., Vodopiutz, J., Rieder, H., Gillessen‐Kaesbach, G., & Kaiser, F. J. (n.d.). hidden Mutations in Cornelia de Lange Syndrome Limitations of Sanger Sequencing in Molecular Diagnostics. Human mutation, 36(1), 26–29. http://access.bl.uk/ark:/81055/vdc_100025063439.0x000062