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Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358901/ https://www.ncbi.nlm.nih.gov/pubmed/28349113 http://dx.doi.org/10.1016/j.jdcr.2017.01.002 |
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author | Goussot, Raphaëlle Prasad, Megana Stoetzel, Corinne Lenormand, Cédric Dollfus, Hélène Lipsker, Dan |
author_facet | Goussot, Raphaëlle Prasad, Megana Stoetzel, Corinne Lenormand, Cédric Dollfus, Hélène Lipsker, Dan |
author_sort | Goussot, Raphaëlle |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-5358901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-53589012017-03-27 Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma Goussot, Raphaëlle Prasad, Megana Stoetzel, Corinne Lenormand, Cédric Dollfus, Hélène Lipsker, Dan JAAD Case Rep Case Series Elsevier 2017-03-19 /pmc/articles/PMC5358901/ /pubmed/28349113 http://dx.doi.org/10.1016/j.jdcr.2017.01.002 Text en © 2016 by the American Academy of Dermatology, Inc. Published by Elsevier, Inc. http://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 Series Goussot, Raphaëlle Prasad, Megana Stoetzel, Corinne Lenormand, Cédric Dollfus, Hélène Lipsker, Dan Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma |
title | Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma |
title_full | Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma |
title_fullStr | Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma |
title_full_unstemmed | Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma |
title_short | Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma |
title_sort | expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by fam111b mutations: report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358901/ https://www.ncbi.nlm.nih.gov/pubmed/28349113 http://dx.doi.org/10.1016/j.jdcr.2017.01.002 |
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