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HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis-related morbidity.
Gurrin LC, Bertalli NA, Dalton GW, Osborne NJ, Constantine CC, McLaren CE, English DR, Gertig DM, Delatycki MB, Nicoll AJ, Southey MC, Hopper JL, Giles GG, Anderson GJ, Olynyk JK, Powell LW, Allen KJ; HealthIron Study Investigators. Gurrin LC, et al. Among authors: delatycki mb. Hepatology. 2009 Jul;50(1):94-101. doi: 10.1002/hep.22972. Hepatology. 2009. PMID: 19554541 Free PMC article.
Clinical and genetic study of Friedreich ataxia in an Australian population.
Delatycki MB, Paris DB, Gardner RJ, Nicholson GA, Nassif N, Storey E, MacMillan JC, Collins V, Williamson R, Forrest SM. Delatycki MB, et al. Am J Med Genet. 1999 Nov 19;87(2):168-74. doi: 10.1002/(sici)1096-8628(19991119)87:2<168::aid-ajmg8>3.0.co;2-2. Am J Med Genet. 1999. PMID: 10533031
Friedreich ataxia: an overview.
Delatycki MB, Williamson R, Forrest SM. Delatycki MB, et al. J Med Genet. 2000 Jan;37(1):1-8. doi: 10.1136/jmg.37.1.1. J Med Genet. 2000. PMID: 10633128 Free PMC article. Review.
Insurance agreement to facilitate genetic testing.
Delatycki M, Allen K, Williamson R. Delatycki M, et al. Lancet. 2002 Apr 20;359(9315):1433. doi: 10.1016/S0140-6736(02)08369-1. Lancet. 2002. PMID: 11978360 No abstract available.
Clinical haemochromatosis in HFE mutation carriers.
Allen KJ, Warner B, Delatycki MB. Allen KJ, et al. Among authors: delatycki mb. Lancet. 2002 Aug 3;360(9330):412-3; author reply 413-4. doi: 10.1016/s0140-6736(02)09583-1. Lancet. 2002. PMID: 12241805 No abstract available.
466 results