The Directory of Open Access Journals
DOAJ Logotype
Open
Global
Trusted
Main actions
Support
Institutions and libraries
Publishers
Institutional and library supporters
Apply
Application form
Guide to applying
The DOAJ Seal
Transparency & best practice
Publisher information
Licensing & copyright
Search
Menu
Secondary actions
Search
Journals
Articles
Documentation
API
OAI-PMH
Widgets
Public data dump
OpenURL
XML
Metadata help
Preservation
About
About DOAJ
DOAJ at 20
DOAJ team
Ambassadors
Advisory Board & Council
Editorial Policy Advisory Group
Volunteers
News
Support
Institutions and libraries
Publishers
Institutional and library supporters
Apply
Application form
Guide to applying
The DOAJ Seal
Transparency & best practice
Publisher information
Licensing & copyright
Login
Login
Quick search
Close
×
Journals
Articles
Search by keywords:
In the field:
In all fields
Title
ISSN
Subject
Publisher
Country of publisher
Search
Frontiers in Genetics
(Apr 2022)
Editorial: Copy Number Variation in Rare Disorders
Katalin Komlósi,
Attila Gyenesei,
Judit Bene
Affiliations
Katalin Komlósi
Institute of Human Genetics, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany
Attila Gyenesei
Bioinformatics Research Group, Genomics and Bioinformatics Core Facility, Szentagothai Research Center, University of Pécs, Pécs, Hungary
Judit Bene
Department of Medical Genetics, Clinical Centre, Medical School, University of Pécs, Pécs, Hungary
DOI
https://doi.org/10.3389/fgene.2022.898059
Journal volume & issue
Vol. 13
Abstract
Read online
No abstracts available.
Keywords
copy number variation (CNV)
rare disorders
genomic disorders
Mendelian disease
genomic rearrangement
WeChat QR code
Close