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Case report of a Li–Fraumeni syndrome-like phenotype with a de novo mutation in CHEK2: Erratum
Formato: | Online Artículo Texto |
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Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266076/ https://www.ncbi.nlm.nih.gov/pubmed/31265670 http://dx.doi.org/10.1097/MD.0000000000005665 |
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collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-5266076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-52660762017-02-06 Case report of a Li–Fraumeni syndrome-like phenotype with a de novo mutation in CHEK2: Erratum Medicine (Baltimore) Erratum Wolters Kluwer Health 2016-12-09 /pmc/articles/PMC5266076/ /pubmed/31265670 http://dx.doi.org/10.1097/MD.0000000000005665 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | Erratum Case report of a Li–Fraumeni syndrome-like phenotype with a de novo mutation in CHEK2: Erratum |
title | Case report of a Li–Fraumeni syndrome-like phenotype with a de novo mutation in CHEK2: Erratum |
title_full | Case report of a Li–Fraumeni syndrome-like phenotype with a de novo mutation in CHEK2: Erratum |
title_fullStr | Case report of a Li–Fraumeni syndrome-like phenotype with a de novo mutation in CHEK2: Erratum |
title_full_unstemmed | Case report of a Li–Fraumeni syndrome-like phenotype with a de novo mutation in CHEK2: Erratum |
title_short | Case report of a Li–Fraumeni syndrome-like phenotype with a de novo mutation in CHEK2: Erratum |
title_sort | case report of a li–fraumeni syndrome-like phenotype with a de novo mutation in chek2: erratum |
topic | Erratum |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266076/ https://www.ncbi.nlm.nih.gov/pubmed/31265670 http://dx.doi.org/10.1097/MD.0000000000005665 |