DEHGHANZAD, Reyhaneh; AGHAJANPOUR MIR, Mohsen; GOLCHEHRE, Zahra; ASADOLLAHI, Mostafa; RAHBAR PARVANEH, Roghayeh; TASHARROFI, Behnoosh; SHAKOORI FARAHANI, Abbas; KERAMATIPOUR, Mohammad. 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: Unraveling 9q Duplication Via Comprehensive Whole Exome Sequencing. Iranian Journal of Child Neurology, [S. l.], v. 20, n. 1, p. 79–84, 2026. DOI: 10.22037/ijcn.v20i1.45486. Disponível em: https://journals.sbmu.ac.ir/ijcn/article/view/45486. Acesso em: 8 jul. 2026.