Comparison of exon-level copy number variants in CytoScan XON assay and next-generation sequencing in clinical samples-Reference-Cited by-同舟云学术

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Comparison of exon-level copy number variants in CytoScan XON assay and next-generation sequencing in clinical samples

Published:2024-06 Issue: Volume:560 Page:119703
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Won Dongju^ORCID,Yeom Eunju,Shin Saeam,Lee Seung‑Tae,Rak Choi Jong

Publisher

Elsevier BV

Reference12 articles.

1. Chromosomal microarray analysis (CMA) a clinical diagnostic tool in the prenatal and postnatal settings;Batzir;Pediatr. Endocrinol. Rev.,2015

2. Additional information from chromosomal microarray analysis (CMA) over conventional karyotyping when diagnosing chromosomal abnormalities in miscarriage: a systematic review and meta-analysis;Dhillon;BJOG,2014

3. Prenatal diagnosis by chromosomal microarray analysis;Levy;Fertil. Steril.,2018

4. Chromosomal microarray in children with developmental delay: the experience of a tertiary center in Korea;Yang;Front. Pediatr.,2021

5. Free-access copy-number variant detection tools for targeted next-generation sequencing data;Roca;Mutat. Res. Rev. Mutat. Res.,2019

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