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Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study

Lilian Downie1,2,3,4, Jane Halliday2,4, Rachel Burt2,4

  • 1Victorian Clinical Genetics Services, Melbourne, VIC, Australia.

European Journal of Human Genetics : EJHG
|November 10, 2020
PubMed
Abstract

No abstract available in PubMed .

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