Showing 1 - 9 results of 9 for search 'Gordon D McLaren', 查询时间: 0.05s
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The D519G Polymorphism of Glyceronephosphate O-Acyltransferase Is a Risk Factor for Familial Porphyria Cutanea Tarda. 由 Colin P Farrell, Jessica R Overbey, Hetanshi Naik, Danielle Nance, Gordon D McLaren, Christine E McLaren, Luming Zhou, Robert J Desnick, Charles J Parker, John D Phillips
出版 2016-01-01
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Prevalence of iron deficiency in 62,685 women of seven race/ethnicity groups: The HEIRS Study. 由 James C Barton, Howard H Wiener, Ronald T Acton, Paul C Adams, John H Eckfeldt, Victor R Gordeuk, Emily L Harris, Christine E McLaren, Helen Harrison, Gordon D McLaren, David M Reboussin
出版 2020-01-01
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Associations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations. 由 Christine E McLaren, Stela McLachlan, Chad P Garner, Chris D Vulpe, Victor R Gordeuk, John H Eckfeldt, Paul C Adams, Ronald T Acton, Joseph A Murray, Catherine Leiendecker-Foster, Beverly M Snively, Lisa F Barcellos, James D Cook, Gordon D McLaren
出版 2012-01-01
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Screening for Iron Overload: Lessons from the HEmochromatosis and IRon Overload Screening (HEIRS) Study 由 Paul C Adams, James C Barton, Gordon D McLaren, Ronald T Acton, Mark Speechley, Christine E McLaren, David M Reboussin, Catherine Leiendecker-Foster, Emily L Harris, Beverly M Snively, Thomas Vogt, Phyliss Sholinsky, Elizabeth Thomson, Fitzroy W Dawkins, Victor R Gordeuk, John H Eckfeldt
出版 2009-01-01
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Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes 由 James C. Barton, Christine E. McLaren, Wen-pin Chen, Grant A. Ramm, Gregory J. Anderson, Lawrie W. Powell, V. Nathan Subramaniam, Paul C. Adams, Pradyumna D. Phatak, Lyle C. Gurrin, John D. Phillips, Charles J. Parker, Mary J. Emond, Gordon D. McLaren
出版 2018-09-01
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Clinical Manifestations of Hemochromatosis in HFE C282Y Homozygotes Identified by Screening 由 Gordon D McLaren, Christine E McLaren, Paul C Adams, James C Barton, David M Reboussin, Victor R Gordeuk, Ronald T Acton, Emily L Harris, Mark R Speechley, Phyliss Sholinsky, Fitzroy W Dawkins, Beverly M Snively, Thomas M Vogt, John H Eckfeldt, for the Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators
出版 2008-01-01
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Genome-wide association study identifies genetic loci associated with iron deficiency. 由 Christine E McLaren, Chad P Garner, Clare C Constantine, Stela McLachlan, Chris D Vulpe, Beverly M Snively, Victor R Gordeuk, Debbie A Nickerson, James D Cook, Catherine Leiendecker-Foster, Kenneth B Beckman, John H Eckfeldt, Lisa F Barcellos, Joseph A Murray, Paul C Adams, Ronald T Acton, Anthony A Killeen, Gordon D McLaren
出版 2011-03-01
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