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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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