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Frontiers in Genetics
(Jul 2023)
Editorial: Next generation sequencing (NGS) for rare diseases diagnosis ‐ Volume II
Xiu-An Yang,
Xiu-An Yang,
Hu Hao,
Hu Hao,
Can Liao
Affiliations
Xiu-An Yang
Laboratory of Genetic Engineering and Genomics, School of Basic Medical Sciences, Chengde Medical University, Chengde, China
Xiu-An Yang
Hebei Key Laboratory of Nerve Injury and Repair, Chengde Medical University, Chengde, China
Hu Hao
Department of Pediatrics, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China
Hu Hao
Inborn Errors of Metabolism Laboratory, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China
Can Liao
Guangzhou Women and Children’s Medical Center, Guangzhou, China
DOI
https://doi.org/10.3389/fgene.2023.1249585
Journal volume & issue
Vol. 14
Abstract
Read online
No abstracts available.
Keywords
next generation sequencing
rare diseases diagnosis
whole-exome sequencing
whole-genome sequencing
copy number variants (CNV) sequencing
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