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Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders

Detalles Bibliográficos
Autores principales:	Hermanns, Pia, Kumorowicz-Czoch, Małgorzata, Pohlenz, Joachim
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Berlin Heidelberg 2015
Materias:	Meeting Abstract
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715207/ http://dx.doi.org/10.1186/2194-7791-2-S1-A9

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