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Editorial: Copy Number Variation in Rare Disorders

Detalles Bibliográficos
Autores principales: Komlósi, Katalin, Gyenesei, Attila, Bene, Judit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016220/
https://www.ncbi.nlm.nih.gov/pubmed/35450215
http://dx.doi.org/10.3389/fgene.2022.898059
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author Komlósi, Katalin
Gyenesei, Attila
Bene, Judit
author_facet Komlósi, Katalin
Gyenesei, Attila
Bene, Judit
author_sort Komlósi, Katalin
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spelling pubmed-90162202022-04-20 Editorial: Copy Number Variation in Rare Disorders Komlósi, Katalin Gyenesei, Attila Bene, Judit Front Genet Genetics Frontiers Media S.A. 2022-04-05 /pmc/articles/PMC9016220/ /pubmed/35450215 http://dx.doi.org/10.3389/fgene.2022.898059 Text en Copyright © 2022 Komlósi, Gyenesei and Bene. 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
Komlósi, Katalin
Gyenesei, Attila
Bene, Judit
Editorial: Copy Number Variation in Rare Disorders
title Editorial: Copy Number Variation in Rare Disorders
title_full Editorial: Copy Number Variation in Rare Disorders
title_fullStr Editorial: Copy Number Variation in Rare Disorders
title_full_unstemmed Editorial: Copy Number Variation in Rare Disorders
title_short Editorial: Copy Number Variation in Rare Disorders
title_sort editorial: copy number variation in rare disorders
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016220/
https://www.ncbi.nlm.nih.gov/pubmed/35450215
http://dx.doi.org/10.3389/fgene.2022.898059
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AT gyeneseiattila editorialcopynumbervariationinraredisorders
AT benejudit editorialcopynumbervariationinraredisorders