Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases
Author:
Funder
Ministry of National Economy, Hungary
Publisher
Elsevier BV
Subject
Applied Microbiology and Biotechnology,General Medicine,Biotechnology,Bioengineering
Reference40 articles.
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3. Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features;Battaglia;Eur. J. Paediatr. Neurol.,2013
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3. Congenital Heart Defects and 22q11.2 Deletion Syndrome: A 20-Year Update and New Insights to Aid Clinical Diagnosis;Journal of Pediatric Genetics;2023-02-17
4. Chromosomal abnormalities in fetuses with congenital heart disease: a meta-analysis;Archives of Gynecology and Obstetrics;2023-01-07
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