Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis

Lisa Ewans(Garvan Institute of Medical Research), Tony Roscioli(New South Wales Department of Health), Mary‐Louise Freckmann(Canberra Hospital), Corrina Walsh(Prince of Wales Hospital), Sulekha Rajagopalan(Liverpool Hospital), Lesley C. Adès(The University of Sydney), Benjamin Kamien(Services Australia), Carolyn Ellaway(The University of Sydney), André E. Minoche(Garvan Institute of Medical Research), Michelle Lipke(Sydney Children's Hospital), David Mowat(New South Wales Department of Health), William Stevenson(The University of Sydney), Clare Puttick(The Francis Crick Institute), Michael Field(Hunter Genetics), Rani Sachdev(Victorian Clinical Genetics Services), Edwin P. Kirk(The University of Sydney), Marcel E. Dinger(The University of Sydney), Lisa Worgan(Liverpool Hospital), Carey‐Anne Evans(New South Wales Department of Health), Elizabeth E. Palmer(The University of Sydney), Velimir Gayevskiy(Rancho BioSciences (United States)), Deborah Schofield(The University of Sydney), Mark J. Cowley(Garvan Institute of Medical Research), George Elakis(New South Wales Department of Health), Marie‐Christine Morel‐Kopp(The University of Sydney), Rupendra Shrestha(Macquarie University), Meredith Wilson(Children's Hospital at Westmead), Ying Zhu(ZheJiang Academy of Agricultural Sciences), Anna Hackett(Hunter Genetics), Alison Colley(Liverpool Hospital), Michael F. Buckley(New South Wales Department of Health), Anne Turner(Medical Research Institute of New Zealand), Alexander P. Drew(Garvan Institute of Medical Research), Linda Goodwin(Nepean Hospital), Anne Ronan(Hunter Genetics)
European Journal of Human Genetics
August 15, 2022
Cited by 123


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