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Al Turki S, Manickaraj AK, Mercer CL, et al. Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans. Am J Hum Genet. 2016;98(3):592doi: 10.1016/j.ajhg.2016.02.016.
Al Turki, S., Manickaraj, A. K., Mercer, C. L., Gerety, S. S., Hitz, M. P., Lindsay, S., D'Alessandro, L. C. A., Swaminathan, G. J., Bentham, J., Arndt, A. K., Louw, J., Breckpot, J., Gewillig, M., Thienpont, B., Abdul-Khaliq, H., Harnack, C., Hoff, K., Kramer, H. H., Schubert, S., Siebert, R., Toka, O., Cosgrove, C., Watkins, H., Lucassen, A. M., O'Kelly, I. M., Salmon, A. P., Bu'Lock, F. A., Granados-Riveron, J., Setchfield, K., Thornborough, C., Brook, J. D., Mulder, B., Klaassen, S., Bhattacharya, S., Devriendt, K., FitzPatrick, D. R., Wilson, D. I., Mital, S., & Hurles, M. E. (2016). Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans. American journal of human genetics, 98(3), 592. https://doi.org/10.1016/j.ajhg.2016.02.016
Al Turki, Saeed, et al. "Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans." American journal of human genetics vol. 98,3 (2016): 592. doi: https://doi.org/10.1016/j.ajhg.2016.02.016
Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S, D'Alessandro LCA, Swaminathan GJ, Bentham J, Arndt AK, Louw J, Breckpot J, Gewillig M, Thienpont B, Abdul-Khaliq H, Harnack C, Hoff K, Kramer HH, Schubert S, Siebert R, Toka O, Cosgrove C, Watkins H, Lucassen AM, O'Kelly IM, Salmon AP, Bu'Lock FA, Granados-Riveron J, Setchfield K, Thornborough C, Brook JD, Mulder B, Klaassen S, Bhattacharya S, Devriendt K, FitzPatrick DR, Wilson DI, Mital S, Hurles ME. Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans. Am J Hum Genet. 2016 Mar 03;98(3):592. doi: 10.1016/j.ajhg.2016.02.016. Epub 2016 Mar 03. PMID: 28863274; PMCID: PMC4800046.
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