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NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome.
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. Cavaliere E, et al. Among authors: marin d. Clin Genet. 2021 Jul;100(1):114-116. doi: 10.1111/cge.13961. Epub 2021 Mar 29. Clin Genet. 2021. PMID: 33778944 Free PMC article.
Identifying environmental sounds: a multimodal mapping study.
Tomasino B, Canderan C, Marin D, Maieron M, Gremese M, D'Agostini S, Fabbro F, Skrap M. Tomasino B, et al. Among authors: marin d, d agostini s. Front Hum Neurosci. 2015 Oct 21;9:567. doi: 10.3389/fnhum.2015.00567. eCollection 2015. Front Hum Neurosci. 2015. PMID: 26539096 Free PMC article.
858 results