Showing results (31-40 of 37) with videos related to
Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Acta Haematologica|January 1, 1992
Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observationsY J Fei, R Oner, G Bözkurt, et al.British Journal of Haematology|April 1, 1995
A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemiaS Hayette, L Morle, M Bozon, et al.British Journal of Haematology|July 1, 1990
A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblingsA Ghanem, B Pothier, J Marechal, et al.Human Genetics|April 1, 1992
Beta S haplotypes in various world populationsC Oner, A J Dimovski, N F Olivieri, et al.International Journal of Laboratory Hematology|March 20, 2016
Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experienceF Ouali, H Siala, A Bibi, et al.Molecular Biology Reports|September 26, 2013
Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patientsL Jouini, C A Sahli, N Laaouini, et al.Molecular Biology Reports|October 16, 2012
Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype associationN Laouini, A Bibi, H Ammar, et al.Pageof 4