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A novel 506kb deletion causing εγδβ thalassemia.
Blood Cells Mol Dis. 2012 Oct 15-Dec 15;49(3-4):121-7. doi: 10.1016/j.bcmd.2012.05.010. Epub 2012 Jun 5.
Blood Cells Mol Dis. 2012.
PMID: 22677107
Whole-exome-sequencing-based discovery of human FADD deficiency.
Bolze A, Byun M, McDonald D, Morgan NV, Abhyankar A, Premkumar L, Puel A, Bacon CM, Rieux-Laucat F, Pang K, Britland A, Abel L, Cant A, Maher ER, Riedl SJ, Hambleton S, Casanova JL.
Bolze A, et al. Among authors: britland a.
Am J Hum Genet. 2010 Dec 10;87(6):873-81. doi: 10.1016/j.ajhg.2010.10.028. Epub 2010 Nov 25.
Am J Hum Genet. 2010.
PMID: 21109225
Free PMC article.
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Leukocytosis as a predictor for progression to haemolytic uraemic syndrome in Escherichia coli O157:H7 infection.
Anjay MA, Anoop P, Britland A.
Anjay MA, et al. Among authors: britland a.
Arch Dis Child. 2007 Sep;92(9):820-3. doi: 10.1136/adc.2007.120972.
Arch Dis Child. 2007.
PMID: 17715449
Free PMC article.
Review.
No abstract available.
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Decreasing paediatric prescribing errors in a district general hospital.
Davey AL, Britland A, Naylor RJ.
Davey AL, et al. Among authors: britland a.
Qual Saf Health Care. 2008 Apr;17(2):146-9. doi: 10.1136/qshc.2006.021212.
Qual Saf Health Care. 2008.
PMID: 18385410
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