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10 积分 2025-07-07 加入
Targeted gene sequencing and hearing follow-up in 7501 newborns reveals an improved strategy for newborn hearing screening
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Newborn Screening for Deafness/Hard of Hearing in the Genomic Era
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Usefulness of current candidate genetic markers to identify childhood cancer patients at risk for platinum-induced ototoxicity: Results of the European PanCareLIFE cohort study
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Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years
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Assessment of Hearing Screening Combined With Limited and Expanded Genetic Screening for Newborns in Nantong, China
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Newborn Screening for Deafness/Hard of Hearing in the Genomic Era
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已完结
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