[1
]
From Murdoch Children's Research Institute (R.O.B., J.O.B., C.A.S., K.P., R.J.L.,
I.E.S., A.T.M.); Departments of Audiology and Speech Pathology (R.O.B., J.O.B., A.T.M.)
and Paediatrics (C.A.S., R.J.L., I.E.S.), University of Melbourne; The Royal Children's
Hospital (C.A.S., K.P., R.J.L., I.E.S., A.T.M.); Victorian Clinical Genetics Service
(C.A.S., K.P.), Parkville, Victoria; Hunter Genetics (H.G.), John Hunter Hospital,
New Lambton Heights, New South Wales; Austin Health (I.E.S.), Heidelberg, Victoria;
and Florey Institute of Neuroscience and Mental Health (I.E.S.), Parkville, Victoria,
Australia.
[2
]
From Murdoch Children's Research Institute (R.O.B., J.O.B., C.A.S., K.P., R.J.L.,
I.E.S., A.T.M.); Departments of Audiology and Speech Pathology (R.O.B., J.O.B., A.T.M.)
and Paediatrics (C.A.S., R.J.L., I.E.S.), University of Melbourne; The Royal Children's
Hospital (C.A.S., K.P., R.J.L., I.E.S., A.T.M.); Victorian Clinical Genetics Service
(C.A.S., K.P.), Parkville, Victoria; Hunter Genetics (H.G.), John Hunter Hospital,
New Lambton Heights, New South Wales; Austin Health (I.E.S.), Heidelberg, Victoria;
and Florey Institute of Neuroscience and Mental Health (I.E.S.), Parkville, Victoria,
Australia. angela.morgan@mcri.edu.au.