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Journal: Int. J. Mol. Sci., 2022
Volume: 23
Number: 1815
1815
Article:
Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome
Authors:
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Aidin Foroutan, Sadegheh Haghshenas, Pratibha Bhai, Michael A. Levy, Jennifer Kerkhof, Haley McConkey, Marcello Niceta, Andrea Ciolfi, Lucia Pedace, Evelina Miele, David Genevieve, Solveig Heide, Mariëlle Alders, Giuseppe Zampino, Giuseppe Merla, Mélanie Fradin, Eric Bieth, Dominique Bonneau, Klaus Dieterich, Patricia Fergelot, Elise Schaefer, Laurence Faivre, Antonio Vitobello, Silvia Maitz, Rita Fischetto, Cristina Gervasini, Maria Piccione, Ingrid van de Laar, Marco Tartaglia, Bekim Sadikovic and Anne-Sophie Lebreadd
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Cite
Foroutan, A.; Haghshenas, S.; Bhai, P.; Levy, M.A.; Kerkhof, J.; McConkey, H.; Niceta, M.; Ciolfi, A.; Pedace, L.; Miele, E.; et al. Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome. Int. J. Mol. Sci. 2022, 23, 1815. https://doi.org/10.3390/ijms23031815
Foroutan A, Haghshenas S, Bhai P, Levy MA, Kerkhof J, McConkey H, Niceta M, Ciolfi A, Pedace L, Miele E, et al. Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome. International Journal of Molecular Sciences. 2022; 23(3):1815. https://doi.org/10.3390/ijms23031815
Chicago/Turabian StyleForoutan, Aidin, Sadegheh Haghshenas, Pratibha Bhai, Michael A. Levy, Jennifer Kerkhof, Haley McConkey, Marcello Niceta, Andrea Ciolfi, Lucia Pedace, Evelina Miele, and et al. 2022. "Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome" International Journal of Molecular Sciences 23, no. 3: 1815. https://doi.org/10.3390/ijms23031815
APA StyleForoutan, A., Haghshenas, S., Bhai, P., Levy, M. A., Kerkhof, J., McConkey, H., Niceta, M., Ciolfi, A., Pedace, L., Miele, E., Genevieve, D., Heide, S., Alders, M., Zampino, G., Merla, G., Fradin, M., Bieth, E., Bonneau, D., Dieterich, K., ... Lebre, A.-S. (2022). Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome. International Journal of Molecular Sciences, 23(3), 1815. https://doi.org/10.3390/ijms23031815
