Associated Papers
Dual Genetic Diagnosis of Prader-Willi Syndrome and TMC1-Related Severe Congenital Hearing Loss: Diagnostic Challenges and Cochlear Implant Outcomes.
Samara P et al.
Diagnostics (basel, Switzerland), 2026
Variant Reclassification in Underrepresented Minority Children With Sensorineural Hearing Loss.
Scaria SM et al.
Ear and Hearing, 0
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