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This page is a summary of: Neuroanatomical anomalies due to a defect in the FGF3 gene, associated with the Labyrinthine Aplasia, Microtia and Microdontia syndrome: insights from the placement of auditory brainstem implants in two siblings, Therapeutic Advances in Rare Disease, January 2024, SAGE Publications,
DOI: 10.1177/26330040241290834.
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