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DISSEQ - Double-blind Exome and Large Gene Panel Sequencing Analyses in the First-Line Diagnosis of 330 Patients with Intellectual Disability (ID): ES Superiority for the Identification of CNV, Variants in New Disease-Causing Genes, and New Candidate Genes, As Well As the Advantage of Possible Prospective Reanalysis

EUROPEAN JOURNAL OF HUMAN GENETICS(2024)

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