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A rare mutation in a patient with Noonan syndrome with multiple lentigines
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238803/ https://www.ncbi.nlm.nih.gov/pubmed/37274147 http://dx.doi.org/10.1016/j.jdcr.2023.04.006 |
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author | Blanco-Cintrón, Manuel E. Pabón-González, Fabiola Sánchez-Flores, Xavier |
author_facet | Blanco-Cintrón, Manuel E. Pabón-González, Fabiola Sánchez-Flores, Xavier |
author_sort | Blanco-Cintrón, Manuel E. |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-10238803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102388032023-06-04 A rare mutation in a patient with Noonan syndrome with multiple lentigines Blanco-Cintrón, Manuel E. Pabón-González, Fabiola Sánchez-Flores, Xavier JAAD Case Rep Case Report Elsevier 2023-04-23 /pmc/articles/PMC10238803/ /pubmed/37274147 http://dx.doi.org/10.1016/j.jdcr.2023.04.006 Text en © 2023 by the American Academy of Dermatology, Inc. Published by Elsevier, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Blanco-Cintrón, Manuel E. Pabón-González, Fabiola Sánchez-Flores, Xavier A rare mutation in a patient with Noonan syndrome with multiple lentigines |
title | A rare mutation in a patient with Noonan syndrome with multiple lentigines |
title_full | A rare mutation in a patient with Noonan syndrome with multiple lentigines |
title_fullStr | A rare mutation in a patient with Noonan syndrome with multiple lentigines |
title_full_unstemmed | A rare mutation in a patient with Noonan syndrome with multiple lentigines |
title_short | A rare mutation in a patient with Noonan syndrome with multiple lentigines |
title_sort | rare mutation in a patient with noonan syndrome with multiple lentigines |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238803/ https://www.ncbi.nlm.nih.gov/pubmed/37274147 http://dx.doi.org/10.1016/j.jdcr.2023.04.006 |
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