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Editorial: Improving medical diagnosis in rare diseases

Detalles Bibliográficos
Autores principales: Linhares, Natália Duarte, Gorman, Kathleen M, Brusco, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486316/
https://www.ncbi.nlm.nih.gov/pubmed/36147485
http://dx.doi.org/10.3389/fgene.2022.974129
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author Linhares, Natália Duarte
Gorman, Kathleen M
Brusco, Alfredo
author_facet Linhares, Natália Duarte
Gorman, Kathleen M
Brusco, Alfredo
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spelling pubmed-94863162022-09-21 Editorial: Improving medical diagnosis in rare diseases Linhares, Natália Duarte Gorman, Kathleen M Brusco, Alfredo Front Genet Genetics Frontiers Media S.A. 2022-09-06 /pmc/articles/PMC9486316/ /pubmed/36147485 http://dx.doi.org/10.3389/fgene.2022.974129 Text en Copyright © 2022 Linhares, Gorman and Brusco. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Linhares, Natália Duarte
Gorman, Kathleen M
Brusco, Alfredo
Editorial: Improving medical diagnosis in rare diseases
title Editorial: Improving medical diagnosis in rare diseases
title_full Editorial: Improving medical diagnosis in rare diseases
title_fullStr Editorial: Improving medical diagnosis in rare diseases
title_full_unstemmed Editorial: Improving medical diagnosis in rare diseases
title_short Editorial: Improving medical diagnosis in rare diseases
title_sort editorial: improving medical diagnosis in rare diseases
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486316/
https://www.ncbi.nlm.nih.gov/pubmed/36147485
http://dx.doi.org/10.3389/fgene.2022.974129
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