ArticleIranian journal of child neurology2026

Decoding the Genetic Enigma: A Case Study on Congenital Anomalies with Developmental Delay and 9q Duplication Unveiled Via Comprehensive Whole Exome Sequencing and Cytogenetic Analysis.

Reyhaneh Dehghanzad et al.PubMed ↗Full text ↗Publisher ↗

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