Articles citing this paper
Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome and spinal muscular atrophy: patterns of community and healthcare provider participation in a Victorian screening program
Ruth Leibowitz 
A * , Sharon Lewis B C , Jon Emery D , John Massie E F G , Melanie Smith H , Martin Delatycki H I J and Alison Archibald J K *
+ Author Affiliations
- Author Affiliations
A Department of General Practice, University of Melbourne, Melbourne, Vic., Australia.
B Department of Paediatrics, Melbourne Medical School, Royal Children’s Hospital, Parkville, Vic., Australia.
C Murdoch Children’s Research Institute, Parkville, Vic., Australia.
D Centre for Cancer Research, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, Vic., Australia.
E Department of Respiratory Medicine, Royal Children’s Hospital, Parkville, Vic., Australia.
F Children’s Bioethics Centre, Parkville, Vic., Australia.
G Department of Paediatrics, Royal Children’s Hospital, University of Melbourne, Murdoch Children’s Research Institute, Parkville, Vic., Australia.
H Victorian Clinical Genetics Services, Parkville, Vic., Australia.
I Bruce Lefroy Centre for Genetic Health Research, Murdoch Children’s Research Institute, Flemington Road, Parkville, Vic. 3052 Australia.
J Department of Paediatrics, University of Melbourne, Parkville, Vic., Australia.
K Victorian Clinical Genetics Services, Murdoch Children’s Research Institute, Melbourne, Vic., Australia.
Australian Journal of Primary Health 28(6) 580-587 https://doi.org/10.1071/PY21247
Submitted: 9 November 2021 Accepted: 3 August 2022 Published: 4 October 2022
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