The Directory of Open Access Journals
DOAJ Logotype
Open
Global
Trusted
Main actions
Support
Institutions and libraries
Publishers
Institutional and library supporters
Funders
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
Funders
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 Medicine
(Sep 2023)
Editorial: Whole Genome Sequencing for rare diseases
Chiara Di Resta,
Chiara Di Resta,
Valeria D'Argenio,
Valeria D'Argenio
Affiliations
Chiara Di Resta
Faculty of Medicine, Vita-Salute San Raffaele University, Milan, Italy
Chiara Di Resta
Genomic Unit for the Diagnosis of Human Pathologies, IRCCS San Raffaele Scientific Institute, Milan, Italy
Valeria D'Argenio
Department of Human Sciences and Quality of Life Promotion, San Raffaele Open University, Rome, Italy
Valeria D'Argenio
CEINGE-Biotecnologie Avanzate Franco Salvatore, Naples, Italy
DOI
https://doi.org/10.3389/fmed.2023.1267930
Journal volume & issue
Vol. 10
Abstract
Read online
No abstracts available.
Keywords
rare diseases
Whole Genome Sequencing
diagnosis
treatment
pathogenesis
WeChat QR code
Close