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Cavaliere E, Gortan AJ, Passon N, et al. NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome. Clin Genet. 2021;100(1):114-116doi: 10.1111/cge.13961.
Cavaliere, E., Gortan, A. J., Passon, N., Fabbro, D., Marin, D., Carecchio, M., Baldan, F., Credendino, S. C., Gallo, R., Cogo, P., Damante, G., & De Vita, G. (2021). NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome. Clinical genetics, 100(1), 114-116. https://doi.org/10.1111/cge.13961
Cavaliere, Elena, et al. "NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome." Clinical genetics vol. 100,1 (2021): 114-116. doi: https://doi.org/10.1111/cge.13961
Cavaliere E, Gortan AJ, Passon N, Fabbro D, Marin D, Carecchio M, Baldan F, Credendino SC, Gallo R, Cogo P, Damante G, De Vita G. NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome. Clin Genet. 2021 Jul;100(1):114-116. doi: 10.1111/cge.13961. Epub 2021 Mar 29. PMID: 33778944; PMCID: PMC8251915.
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