Diagnostic Yield of Next-Generation Sequencing for Rare Pediatric Genetic Disorders: A Single-Center Experience

<b>Background:</b> Next-generation sequencing (NGS), particularly whole-exome sequencing (WES), has become a powerful diagnostic tool for rare genetic conditions. However, its success rate varies based on the underlying genetic etiology and the population studied. <b>Methods</b&...

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Bibliographic Details
Main Authors: Milena Stoyanova, Dinnar Yahya, Mari Hachmeriyan, Mariya Levkova
Format: Article
Language:English
Published: MDPI AG 2025-06-01
Series:Medical Sciences
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Online Access:https://www.mdpi.com/2076-3271/13/2/75
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