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Škorić-Milosavljević D, Lahrouchi N, Bosada FM, et al. Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot. Genet Med. 2021;23(10):2013doi: 10.1038/s41436-021-01279-7.
Škorić-Milosavljević, D., Lahrouchi, N., Bosada, F. M., Dombrowsky, G., Williams, S. G., Lesurf, R., Tjong, F. V. Y., Walsh, R., El Bouchikhi, I., Breckpot, J., Audain, E., Ilgun, A., Beekman, L., Ratbi, I., Strong, A., Muenke, M., Heide, S., Muir, A. M., Hababa, M., Cross, L., Zhou, D., Pastinen, T., Zackai, E., Atmani, S., Ouldim, K., Adadi, N., Steindl, K., Rauch, A., Brook, D., Wilsdon, A., Kuipers, I., Blom, N. A., Mulder, B. J., Mefford, H. C., Keren, B., Joset, P., Kruszka, P., Thiffault, I., Sheppard, S. E., Roberts, A., Lodder, E. M., Keavney, B. D., Clur, S. B., Mital, S., Hitz, M. P., Christoffels, V. M., Postma, A. V., & Bezzina, C. R. (2021). Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot. Genetics in medicine : official journal of the American College of Medical Genetics, 23(10), 2013. https://doi.org/10.1038/s41436-021-01279-7
Škorić-Milosavljević, Doris, et al. "Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot." Genetics in medicine : official journal of the American College of Medical Genetics vol. 23,10 (2021): 2013. doi: https://doi.org/10.1038/s41436-021-01279-7
Škorić-Milosavljević D, Lahrouchi N, Bosada FM, Dombrowsky G, Williams SG, Lesurf R, Tjong FVY, Walsh R, El Bouchikhi I, Breckpot J, Audain E, Ilgun A, Beekman L, Ratbi I, Strong A, Muenke M, Heide S, Muir AM, Hababa M, Cross L, Zhou D, Pastinen T, Zackai E, Atmani S, Ouldim K, Adadi N, Steindl K, Rauch A, Brook D, Wilsdon A, Kuipers I, Blom NA, Mulder BJ, Mefford HC, Keren B, Joset P, Kruszka P, Thiffault I, Sheppard SE, Roberts A, Lodder EM, Keavney BD, Clur SB, Mital S, Hitz MP, Christoffels VM, Postma AV, Bezzina CR. Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot. Genet Med. 2021 Oct;23(10):2013. doi: 10.1038/s41436-021-01279-7. PMID: 34522030; PMCID: PMC8486656.
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