Gelman, H., Dines, J. N., Berg, J., Berger, A. H., Brnich, S., Hisama, F. M., . . . Starita, L. M. (2019). Recommendations for the collection and use of multiplexed functional data for clinical variant interpretation. Genome Med.
Style de citation ChicagoGelman, Hannah, et al. "Recommendations for the Collection and Use of Multiplexed Functional Data for Clinical Variant Interpretation." Genome Med 2019.
Style de citation MLAGelman, Hannah, et al. "Recommendations for the Collection and Use of Multiplexed Functional Data for Clinical Variant Interpretation." Genome Med 2019.
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