Showing results (1-10 of 24) with videos related to
Sort By:
Pageof 3
World Journal of Microbiology & Biotechnology|January 14, 2014
Polymerase chain Reaction in molecular biotechnology; appropriate technology for developing countriesA E Felice, C AlshinawiBlood|October 1, 1984
Partial deletion of the 5' beta-globin gene region causes beta zero-thalassemia in members of an American black familyB J Padanilam, A E Felice, T H HuismanBiochemical Genetics|June 1, 1981
Alpha-thalassemia and the production of different alpha chain variants in heterozygotesA E Felice, B B Webber, T H HuismanHemoglobin|May 21, 1999
Characterization and locus assignment of two alpha-globin variants present in the Maltese population: Hb St. Luke's [alpha95(G2)Pro-->Arg] and Hb Setif [alpha94(G1)Asp-->Tyr]S Bezzina Wettinger, R Galdies, C Scerri, et al.Experimental Hematology|February 1, 1989
Quantitation of erythropoietin stimulatory activity using [3H]thymidine uptake by K562 cellsJ P Lewis, V C McKie, G B Faguet, et al.American Journal of Clinical Pathology|July 1, 1981
The occurrence and identification of alpha-thalassemia-2 among hemoglobin S heterozygotesA E Felice, C A Altay, P F Milner, et al.Blood|May 1, 1984
The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genesA E Felice, M P Cleek, K McKie, et al.Hemoglobin|January 1, 1984
Alternate organization of alpha G-Philadelphia globin genes among U.S. black and Italian Caucasian heterozygotesG V Sciarratta, G Sansone, G Ivaldi, et al.Hemoglobin|January 1, 1981
Clinical and hematological evaluation of two delta 0 beta 0-thalassemia homozygotesG Dincol, C Altay, M Aksoy, et al.British Journal of Pharmacology|April 28, 2001
Mutation screening of the muscarinic M(2) and M(3) receptor genes in normal and asthmatic subjectsA G Fenech, M J Ebejer, A E Felice, et al.Pageof 3