Insufficient Referral for Genetic Counseling in the Management of Hereditary Haemochromatosis in Portugal: A Study of Perceptions of Health Professionals Requesting HFE Genotyping
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://link.springer.com/content/pdf/10.1007/s10897-013-9681-4
Reference24 articles.
1. Adams, P. C., Reboussin, D. M., Barton, J. C., McLaren, C. E., Eckfeldt, J. H., McLaren, G. D., et al. (2005). Hemochromatosis and iron-overload screening in a racially diverse population. New England Journal of Medicine, 352, 1769–1778.
2. Aleman, S., Endalib, S., Stål, P., Lööf, L., Lindgren, S., Sandberg-Gertzén, H., et al. (2011). Health check-ups and family screening allow detection of hereditary hemochromatosis with less advanced liver fibrosis and survival comparable with the general population. Scandinavian Journal of Gastroenterology, 46, 1118–1126.
3. Baars, M. J., Henneman, L., & Ten Kate, L. P. (2005a). Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: a global problem. Genetics in Medicine, 7(9), 605–610.
4. Baars, M. J., Scherpbier, A. J., Schuwirth, L. W., Henneman, L., Beemer, F. A., Cobben, J. M., et al. (2005b). Deficient knowledge of genetics relevant for daily practice among medical students nearing graduation. Genetics in Medicine, 7(5), 295–301.
5. Burke, S., Stone, A., Bedward, J., Thomas, H., & Farndon, P. (2006). A “neglect part of the curriculum” or “of limited use”? Views on genetics training by nongenetics medical trainees and implications for delivery. Genetics in Medicine, 8, 109–115.
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