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A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort.

Pubmed ID: 
29637142
Year: 
2017
Volume: 
1
Issue: 
1
Citation: 
Downie L, Halliday JL, Burt RA, Lunke S, Lynch E, Martyn M, Poulakis Z, Gaff C, Sung V, Wake M, Hunter M, Saunders K, Rose E, Rehm HL, Amor DJ. A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort. BMJ paediatrics open 1 (1) : e000119(2017) PubMed