Exome Sequencing In Infants With Congenital Hearing Impairment: A Population-Based Cohort Study (Vol 28, Pg 587, 2020)
EUROPEAN JOURNAL OF HUMAN GENETICS(2021)
Abstract
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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Key words
Disease genetics,Medical genomics,Biomedicine,general,Human Genetics,Bioinformatics,Gene Expression,Cytogenetics
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