Article

Novel 22q11.2 Deletions Detection Assay Using Gel Electrophoresis

2025-12-01

Abstract excerpt

<h4>Background: </h4> 22q11.2 deletion syndrome (22q11.2DS), also known as Di-George/velocardiofacial syndrome is the most common chromosomal microdeletion and is frequently associated with conotruncal congenital heart defects (CHD). A novel protocol for 22q11.2 deletions detection using conventional PCR and agarose gel electrophoresis was developed, and seven primer pairs targeting six 22q11.2 genes (HIRA, TBX1,...

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Literature Corpus work: 86c2a0bb-af6b-57e0-a64d-b6ab93d9fac2
DOI: 10.20944/preprints202512.0052.v1

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