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Navegación por Autor Moya, Christian M.
Mostrando resultados 1 a 2 de 2
Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
openAccess | | may-2006 | Functional study of a novel single deletion in the TITF1/NKX2.1 homeobox gene that produces congenital hypothyroidism and benign chorea but not pulmonary distress | Moya, Christian M. CSIC; Santisteban, Pilar CSIC ORCID | artículo |
closedAccess | | 2018 | TAZ/WWTR1 mediates the pulmonary effects of NKX2-1 mutations in brain-lung-thyroid syndrome | Moya, Christian M. CSIC; Zaballos, Miguel A. CSIC ORCID; Garzón, Lucía; Luna, Carmen; Simón, Rogelio; Yaffe, Michael B.; Gallego, Elena; Santisteban, Pilar CSIC ORCID; Moreno, José C. | artículo |