Optical Genome Mapping in Prenatal Diagnosis: Democratizing Comprehensive Cytogenomic Testing-Reference-Cited by-同舟云学术

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Optical Genome Mapping in Prenatal Diagnosis: Democratizing Comprehensive Cytogenomic Testing

Published:2024-05-07 Issue:6 Volume:70 Page:783-785
ISSN:0009-9147
Container-title:Clinical Chemistry
language:en
Short-container-title:

Author:

Mathew Mariam T¹²³,Akkari Yassmine M N¹²^ORCID

Affiliation:

1. The Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children’s Hospital , Columbus, OH , United States

2. Department of Pathology, The Ohio State University, Columbus , OH , United States

3. Department of Pediatrics, The Ohio State University , Columbus, OH , United States

Publisher

Oxford University Press (OUP)

Link

https://academic.oup.com/clinchem/article-pdf/70/6/783/58985510/hvae060.pdf

Reference13 articles.

1. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study;Lord;Lancet,2019

2. Chromosomal microarray versus karyotyping for prenatal diagnosis;Wapner;N Engl J Med,2012

3. Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study;Petrovski;Lancet,2019

4. Optical genome mapping for prenatal diagnosis: a prospective study;Goumy;Clin Chim Acta,2023

5. Clinical validation and diagnostic utility of optical genome mapping in prenatal diagnostic testing;Sahajpal;J Mol Diagn,2023

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