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

Pubmed ID: 
31827275
Year: 
2019
Month: 
Dec
Citation: 
Downie L, Halliday J, Burt R, Lunke S, Lynch E, Martyn M, Poulakis Z, Gaff C, Sung V, Wake M, Hunter MF, Saunders K, Rose E, Lewis S, Jarmolowicz A, Phelan D, Rehm HL, Melbourne Genomics Health Alliance, Amor DJ. Exome sequencing in infants with congenital hearing impairment: a population-based cohort study. European journal of human genetics : EJHG (2019) PubMed