This page shows the publications Pierre Zalloua has written about Mutation.
WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon. Hum Mol Genet. 2008 Dec 15; 17(24):4012-21.
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.
Molecular basis of oculocutaneous albinism type 1 in Lebanese patients. J Hum Genet. 2005; 50(6):317-319.
Frequency of the CCR5-delta 32 chemokine receptor gene mutation in the Lebanese population. East Mediterr Health J. 2004 Jul-Sep; 10(4-5):671-5.
Origin and history of the IVS-I-110 and codon 39 beta-thalassemia mutations in the Lebanese population. Hum Biol. 2002 Dec; 74(6):837-47.
Boston type I keratoprosthesis for treatment of gelatinous drop-like corneal dystrophy after repeated graft failure. Semin Ophthalmol. 2015 Mar; 30(2):150-3.
A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient. Eur J Hum Genet. 2014 Jan; 22(1):140-3.
Increase of satellite tobacco ringspot virus RNA initiated by inoculating circular RNA. Virology. 1995 Apr 20; 208(2):832-7.
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