Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project

Genetics in Medicine, Published online: 24 January 2020; doi:10.1038/s41436-019-0745-1Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project

Source: Genetics in Medicine - January 23, 2020 Category: Genetics & Stem Cells Authors: Lilian Downie Jane Halliday Sharon Lewis Sebastian Lunke Elly Lynch Melissa Martyn Clara Gaff Anna Jarmolowicz David J. Amor Source Type: research