APA (7th ed.) Citation

Fischer, J., Alders, M., Mannens, M. M. A. M., Genevieve, D., Hackmann, K., Schröck, E., . . . Porrmann, J. Validation of a hypomorphic variant in CDK13 as the cause of CHDFIDD with autosomal recessive inheritance through determination of an episignature. BMC.

Chicago Style (17th ed.) Citation

Fischer, Jan, Mariëlle Alders, Marcel M. A. M. Mannens, David Genevieve, Karl Hackmann, Evelin Schröck, Bekim Sadikovic, and Joseph Porrmann. Validation of a Hypomorphic Variant in CDK13 as the Cause of CHDFIDD with Autosomal Recessive Inheritance Through Determination of an Episignature. BMC.

MLA (9th ed.) Citation

Fischer, Jan, et al. Validation of a Hypomorphic Variant in CDK13 as the Cause of CHDFIDD with Autosomal Recessive Inheritance Through Determination of an Episignature. BMC.