Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests.

Autor: Archibald AD; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia., Smith MJ; Victorian Clinical Genetics Services, Parkville, Victoria, Australia. melanie.smith@vcgs.org.au.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia. melanie.smith@vcgs.org.au., Burgess T; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia., Scarff KL; Victorian Clinical Genetics Services, Parkville, Victoria, Australia., Elliott J; Victorian Clinical Genetics Services, Parkville, Victoria, Australia., Hunt CE; Victorian Clinical Genetics Services, Parkville, Victoria, Australia., Barns-Jenkins C; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia., Holt C; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia., Sandoval K; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia., Kumar VS; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia., Ward L; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia., Allen EC; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia., Collis SV; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia., Cowie S; Victorian Clinical Genetics Services, Parkville, Victoria, Australia., Francis D; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia., Delatycki MB; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Royal Children's Hospital, Parkville, Victoria, Australia., Yiu EM; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Royal Children's Hospital, Parkville, Victoria, Australia., Massie RJ; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Royal Children's Hospital, Parkville, Victoria, Australia., Pertile MD; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia., du Sart D; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia., Bruno D; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia., Amor DJ; Victorian Clinical Genetics Services, Parkville, Victoria, Australia.; Murdoch Childrens Research Institute, Parkville, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.; Royal Children's Hospital, Parkville, Victoria, Australia.
Jazyk: angličtina
Zdroj: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2018 Nov; Vol. 20 (11), pp. 1485.
DOI: 10.1038/gim.2017.266
Abstrakt: Zoe McDonald, BSc, was omitted from the list of article coauthors. Her name should have been included as the seventh author, following Clare Elizabeth Hunt. Her affiliation is Victorian Clinical Genetics Services, Parkville, Victoria, Australia. The authors regret the error.
Databáze: MEDLINE
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