April 3, 2020
Findings from the Melbourne Genomics Congenital Deafness Clinical Flagship have been published in two notable peer-reviewed journals. One of 16 clinical projects, the Deafness Flagship investigated the impact of genomic testing on the care of babies born with hearing loss.
March 9, 2020
Results from the Melbourne Genomics clinical project investigating the impact of genomic testing for the heart condition dilated cardiomyopathy (DCM) have now been published.
February 25, 2020
A new podcast now available from ABC Radio National’s Big Ideas program, ‘Is genomic medicine delivering on its potential?’ was recorded at a Melbourne Genomics public forum held late last year.
January 24, 2020
A Melbourne Genomics study published today in Genetics in Medicine has found that more than two-thirds (68 per cent) of parents who consented to genomic testing for hearing loss genes for their infant also accepted the offer of additional screening of the genome for a range of child-onset conditions.