NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome

[Image: see text]

Detalles Bibliográficos
Autores principales: Cavaliere, Elena, Gortan, Anna Jolanda, Passon, Nadia, Fabbro, Dora, Marin, Dario, Carecchio, Miryam, Baldan, Federica, Credendino, Sara Carmela, Gallo, Rosa, Cogo, Paola, Damante, Giuseppe, De Vita, Gabriella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2021
Materias:
Letters to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251915/
https://www.ncbi.nlm.nih.gov/pubmed/33778944
http://dx.doi.org/10.1111/cge.13961
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author Cavaliere, Elena
Gortan, Anna Jolanda
Passon, Nadia
Fabbro, Dora
Marin, Dario
Carecchio, Miryam
Baldan, Federica
Credendino, Sara Carmela
Gallo, Rosa
Cogo, Paola
Damante, Giuseppe
De Vita, Gabriella
author_facet Cavaliere, Elena
Gortan, Anna Jolanda
Passon, Nadia
Fabbro, Dora
Marin, Dario
Carecchio, Miryam
Baldan, Federica
Credendino, Sara Carmela
Gallo, Rosa
Cogo, Paola
Damante, Giuseppe
De Vita, Gabriella
author_sort Cavaliere, Elena
collection PubMed
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spelling pubmed-82519152021-07-07 NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome Cavaliere, Elena Gortan, Anna Jolanda Passon, Nadia Fabbro, Dora Marin, Dario Carecchio, Miryam Baldan, Federica Credendino, Sara Carmela Gallo, Rosa Cogo, Paola Damante, Giuseppe De Vita, Gabriella Clin Genet Letters to the Editor [Image: see text] Blackwell Publishing Ltd 2021-03-29 2021-07 /pmc/articles/PMC8251915/ /pubmed/33778944 http://dx.doi.org/10.1111/cge.13961 Text en © 2021 The Authors. Clinical Genetics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters to the Editor
Cavaliere, Elena
Gortan, Anna Jolanda
Passon, Nadia
Fabbro, Dora
Marin, Dario
Carecchio, Miryam
Baldan, Federica
Credendino, Sara Carmela
Gallo, Rosa
Cogo, Paola
Damante, Giuseppe
De Vita, Gabriella
NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome
title NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome
title_full NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome
title_fullStr NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome
title_full_unstemmed NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome
title_short NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome
title_sort nkx2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251915/
https://www.ncbi.nlm.nih.gov/pubmed/33778944
http://dx.doi.org/10.1111/cge.13961
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