The uncertainty of copy number variants: pregnancy decisions and clinical follow-up
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference18 articles.
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2. Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes;Liang;Genet Med,2019
3. Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes;Liang;J Mol Diagn,2014
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5. Chromosomal microarray versus karyotyping for prenatal diagnosis;Wapner;N Engl J Med,2012
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3. Perinatal outcomes after a prenatal diagnosis of a fetal copy number variant: a retrospective population-based cohort study;BMC Pediatrics;2024-08-22
4. Chromosomal Microarray Analysis in Fetuses with Ultrasound Abnormalities;International Journal of General Medicine;2024-08
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