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

Pubmed ID: 
31974413
Year: 
2020
Month: 
Jan
Citation: 
Downie L, Halliday J, Lewis S, Lunke S, Lynch E, Martyn M, Gaff C, Jarmolowicz A, Amor DJ. Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project. Genetics in medicine : official journal of the American College of Medical Genetics (2020) PubMed