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Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731975/ https://www.ncbi.nlm.nih.gov/pubmed/36505034 http://dx.doi.org/10.1016/j.jdcr.2022.10.034 |
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author | Trupiano, Nicole Koeppe, Erika Jacobs, Michelle F. Else, Tobias Cha, Kelly B. |
author_facet | Trupiano, Nicole Koeppe, Erika Jacobs, Michelle F. Else, Tobias Cha, Kelly B. |
author_sort | Trupiano, Nicole |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-9731975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97319752022-12-10 Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants Trupiano, Nicole Koeppe, Erika Jacobs, Michelle F. Else, Tobias Cha, Kelly B. JAAD Case Rep Case Report Elsevier 2022-11-07 /pmc/articles/PMC9731975/ /pubmed/36505034 http://dx.doi.org/10.1016/j.jdcr.2022.10.034 Text en © 2022 Published by Elsevier on behalf of the American Academy of Dermatology, Inc. This is an open access.. 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 Trupiano, Nicole Koeppe, Erika Jacobs, Michelle F. Else, Tobias Cha, Kelly B. Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants |
title | Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants |
title_full | Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants |
title_fullStr | Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants |
title_full_unstemmed | Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants |
title_short | Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants |
title_sort | rare presentations can suggest more than one rare condition: striking personal and family cancer history in a patient with both cdkn2a and brca1 pathogenic variants |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731975/ https://www.ncbi.nlm.nih.gov/pubmed/36505034 http://dx.doi.org/10.1016/j.jdcr.2022.10.034 |
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