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Archibald AD, Smith MJ, Burgess T, et al. Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests. Genet Med. 2018;20(11):1485doi: 10.1038/gim.2017.266.
Archibald, A. D., Smith, M. J., Burgess, T., Scarff, K. L., Elliott, J., Hunt, C. E., Barns-Jenkins, C., Holt, C., Sandoval, K., Kumar, V. S., Ward, L., Allen, E. C., Collis, S. V., Cowie, S., Francis, D., Delatycki, M. B., Yiu, E. M., Massie, R. J., Pertile, M. D., du Sart, D., Bruno, D., & Amor, D. J. (2018). Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests. Genetics in medicine : official journal of the American College of Medical Genetics, 20(11), 1485. https://doi.org/10.1038/gim.2017.266
Archibald, Alison Dalton, et al. "Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests." Genetics in medicine : official journal of the American College of Medical Genetics vol. 20,11 (2018): 1485. doi: https://doi.org/10.1038/gim.2017.266
Archibald AD, Smith MJ, Burgess T, Scarff KL, Elliott J, Hunt CE, Barns-Jenkins C, Holt C, Sandoval K, Kumar VS, Ward L, Allen EC, Collis SV, Cowie S, Francis D, Delatycki MB, Yiu EM, Massie RJ, Pertile MD, du Sart D, Bruno D, Amor DJ. Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests. Genet Med. 2018 Nov;20(11):1485. doi: 10.1038/gim.2017.266. PMID: 29388943.
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Genet Med. 2018 Nov;20(11):1485. doi: 10.1038/gim.2017.266.

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

Genetics in medicine : official journal of the American College of Medical Genetics

Alison Dalton Archibald, Melanie Jane Smith, Trent Burgess, Katrina Louise Scarff, Justine Elliott, Clare Elizabeth Hunt, Caitlin Barns-Jenkins, Chelsea Holt, Karina Sandoval, Vanessa Siva Kumar, Lisa Ward, Emily Caroline Allen, Sarah Valerie Collis, Shannon Cowie, David Francis, Martin B Delatycki, Eppie Mildred Yiu, R John Massie, Mark Domenic Pertile, Desirée du Sart, Damien Bruno, David J Amor

Affiliations

  1. Victorian Clinical Genetics Services, Parkville, Victoria, Australia.
  2. Murdoch Childrens Research Institute, Parkville, Victoria, Australia.
  3. Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.
  4. Victorian Clinical Genetics Services, Parkville, Victoria, Australia. [email protected].
  5. Murdoch Childrens Research Institute, Parkville, Victoria, Australia. [email protected].
  6. Royal Children's Hospital, Parkville, Victoria, Australia.

PMID: 29388943 DOI: 10.1038/gim.2017.266

Abstract

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.

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