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HAMP promoter mutation nc.-153C>T in 785 HEIRS study participants.
Haematologica. 2009 Oct;94(10):1465; author reply 1465-6. doi: 10.3324/haematol.2009.011486.
Haematologica. 2009.
PMID: 19794094
Free PMC article.
Clinical Trial.
No abstract available.
Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening.
McLaren GD, McLaren CE, Adams PC, Barton JC, Reboussin DM, Gordeuk VR, Acton RT, Harris EL, Speechley MR, Sholinsky P, Dawkins FW, Snively BM, Vogt TM, Eckfeldt JH; Hemochromatosis and Iron Overload Screen (HEIRS) Study Research Investigators.
McLaren GD, et al.
Can J Gastroenterol. 2008 Nov;22(11):923-30. doi: 10.1155/2008/907356.
Can J Gastroenterol. 2008.
PMID: 19018338
Free PMC article.
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Thyroid-stimulating hormone and free thyroxine levels in persons with HFE C282Y homozygosity, a common hemochromatosis genotype: the HEIRS study.
Barton JC, Leiendecker-Foster C, Reboussin DM, Adams PC, Acton RT, Eckfeldt JH; Hemochromatosis and Iron Overload Screening Study Research Investigators.
Barton JC, et al.
Thyroid. 2008 Aug;18(8):831-8. doi: 10.1089/thy.2008.0091.
Thyroid. 2008.
PMID: 18651828
Free PMC article.
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Low-density addressable array for the detection and typing of the human papillomavirus.
Delrio-Lafreniere SA, Browning MK, McGlennen RC.
Delrio-Lafreniere SA, et al.
Diagn Microbiol Infect Dis. 2004 Jan;48(1):23-31. doi: 10.1016/j.diagmicrobio.2003.09.007.
Diagn Microbiol Infect Dis. 2004.
PMID: 14761718
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Simultaneous allele-specific amplification: a strategy using modified primer-template mismatches for SNP detection--application to prothrombin 20210A (factor II) and factor V Leiden (1691A) gene mutations.
DelRio-LaFreniere SA, McGlennen RC.
DelRio-LaFreniere SA, et al.
Mol Diagn. 2001 Sep;6(3):201-9. doi: 10.1007/BF03262054.
Mol Diagn. 2001.
PMID: 11571714
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