Associated Papers
A Case of CHARGE Syndrome with a Novel Intronic Variant in the CHD7 Gene.
Kaya E et al.
Journal of Clinical Research in Pediatric Endocrinology, 2025
A Preterm Infant with Multiple Anomalies Diagnosed with Atypical CHARGE Syndrome after a Novel CHD7 Variant Confirmed Using Whole-Genome Sequencing.
Kim HH et al.
Neonatology, 2020
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