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Page 1
Polarized x-rays from a magnetar.
Science. 2022 Nov 11;378(6620):646-650. doi: 10.1126/science.add0080. Epub 2022 Nov 3.
Science. 2022.
PMID: 36356124
Molecular epidemiology of erythropoietic protoporphyria in the U.K.
Whatley SD, Mason NG, Holme SA, Anstey AV, Elder GH, Badminton MN.
Whatley SD, et al. Among authors: mason ng.
Br J Dermatol. 2010 Mar;162(3):642-6. doi: 10.1111/j.1365-2133.2010.09631.x. Epub 2010 Jan 22.
Br J Dermatol. 2010.
PMID: 20105171
Item in Clipboard
Autosomal recessive erythropoietic protoporphyria in the United Kingdom: prevalence and relationship to liver disease.
Whatley SD, Mason NG, Khan M, Zamiri M, Badminton MN, Missaoui WN, Dailey TA, Dailey HA, Douglas WS, Wainwright NJ, Elder GH.
Whatley SD, et al. Among authors: mason ng.
J Med Genet. 2004 Aug;41(8):e105. doi: 10.1136/jmg.2003.016121.
J Med Genet. 2004.
PMID: 15286165
Free PMC article.
No abstract available.
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Gene dosage analysis identifies large deletions of the FECH gene in 10% of families with erythropoietic protoporphyria.
Whatley SD, Mason NG, Holme SA, Anstey AV, Elder GH, Badminton MN.
Whatley SD, et al. Among authors: mason ng.
J Invest Dermatol. 2007 Dec;127(12):2790-4. doi: 10.1038/sj.jid.5700924. Epub 2007 Jun 28.
J Invest Dermatol. 2007.
PMID: 17597821
Free article.
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Pseudoexon activation in the HMBS gene as a cause of the nonerythroid form of acute intermittent porphyria.
Whatley SD, Mason NG, Rhodes JM, Stewart MF, Reed P, Crowley V, Darby CM, Badminton MN.
Whatley SD, et al. Among authors: mason ng.
Clin Chem. 2013 Jul;59(7):1123-5. doi: 10.1373/clinchem.2012.199117. Epub 2013 Apr 22.
Clin Chem. 2013.
PMID: 23609978
No abstract available.
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Ferrochelatase gene polymorphism analysis for accurate genetic counselling in erythropoietic protoporphyria.
Morris SD, Mason NG, Elder GH, Hawk JL, Sarkany RP.
Morris SD, et al. Among authors: mason ng.
Br J Dermatol. 2002 Sep;147(3):572-4. doi: 10.1046/j.1365-2133.2002.04876.x.
Br J Dermatol. 2002.
PMID: 12207604
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Diagnostic strategies for autosomal dominant acute porphyrias: retrospective analysis of 467 unrelated patients referred for mutational analysis of the HMBS, CPOX, or PPOX gene.
Whatley SD, Mason NG, Woolf JR, Newcombe RG, Elder GH, Badminton MN.
Whatley SD, et al. Among authors: mason ng.
Clin Chem. 2009 Jul;55(7):1406-14. doi: 10.1373/clinchem.2008.122564. Epub 2009 May 21.
Clin Chem. 2009.
PMID: 19460837
Free article.
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