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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author Hermanns, Pia
Kumorowicz-Czoch, Małgorzata
Pohlenz, Joachim
author_facet Hermanns, Pia
Kumorowicz-Czoch, Małgorzata
Pohlenz, Joachim
author_sort Hermanns, Pia
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spelling pubmed-47152072016-01-31 Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders Hermanns, Pia Kumorowicz-Czoch, Małgorzata Pohlenz, Joachim Mol Cell Pediatr Meeting Abstract Springer Berlin Heidelberg 2015-07-01 /pmc/articles/PMC4715207/ http://dx.doi.org/10.1186/2194-7791-2-S1-A9 Text en © Hermanns et al. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Meeting Abstract
Hermanns, Pia
Kumorowicz-Czoch, Małgorzata
Pohlenz, Joachim
Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders
title Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders
title_full Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders
title_fullStr Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders
title_full_unstemmed Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders
title_short Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders
title_sort mutations in the nkx2.1 and the pax8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders
topic Meeting Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715207/
http://dx.doi.org/10.1186/2194-7791-2-S1-A9
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AT kumorowiczczochmałgorzata mutationsinthenkx21andthepax8genesinaboywiththyroiddysgenesisrespiratoryandneurologicaldisorders
AT pohlenzjoachim mutationsinthenkx21andthepax8genesinaboywiththyroiddysgenesisrespiratoryandneurologicaldisorders

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