This page shows the publications Pierre Zalloua has written about Globins.
Genetic heterogeneity of Beta thalassemia in Lebanon reflects historic and recent population migration. Ann Hum Genet. 2005 Jan; 69(Pt 1):55-66.
Accurate and rapid prenatal diagnosis of the most frequent East Mediterranean beta-thalassemia mutations. Am J Hematol. 2004 Apr; 75(4):220-4.
Beta-globin gene cluster haplotypes and HbF levels are not the only modulators of sickle cell disease in Lebanon. Eur J Haematol. 2003 Feb; 70(2):79-83.
The codons 8/9 (+G) mutation found for the first time in the Lebanese population. Hemoglobin. 2003 Feb; 27(1):1-5.
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