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Hemoglobin|September 22, 2010
Thalassemia syndromes in Serbia: an updateMilena Radmilovic, Branka Zukic, Biljana Stankovic, et al.Hemoglobin|July 21, 2010
Identification of a new mutation on the beta-globin gene: codons 8/9 (+AGAA); GAG.AAG.TCT(Glu-Lys-Ser)>GAG. AAAGAAG, in a patient from the north of France with a phenotype of beta-thalassemia minorAnne France Georgel, Claude Méreau, Christophe Willekens, et al.Hemoglobin|July 21, 2010
Hydrops fetalis associated with homozygosity for Hb Adana [alpha59(E8)Gly-->Asp (alpha2)]Ita M Nainggolan, Alida Harahap, Iswari SetianingsihHemoglobin|July 21, 2010
Hb Koya Dora [alpha142, Term-->Ser (TAA>TCA in alpha2)]: a rare mutation of the alpha2 gene stop codon associated with alpha-thalassemiaStephen O Brennan, Sheila Ryken, Tim ChanHemoglobin|August 7, 2009
An electronic infrastructure for research and treatment of the thalassemias and other hemoglobinopathies: the Euro-mediterranean ITHANET projectCarsten W Lederer, A Nazli Basak, Yesim Aydinok, et al.Hemoglobin|August 7, 2009
Three new beta-thalassemia mutations with varying degrees of severityHannes Frischknecht, Fabrizio Dutly, Lynda Walker, et al.Hemoglobin|August 7, 2009
Frequency of background and radiation-induced apoptosis in leukocytes of individuals with alpha-thalassemia variants, assessed by the neutral comet assayAlireza Tarang, Hossein Mozdarani, Mohamad T AkbariHemoglobin|August 7, 2009
A second case of Hb Fontainebleau [alpha21(B2)Ala-->Pro] in an individual with microcytosisStephen O Brennan, Tim Chan, Sheila Ryken, et al.Hemoglobin|August 7, 2009
First identification of a point mutation at position -83 (G>A) of the beta-globin gene promoterEstelle Cadet, Karine Foulon, Jean-François Claisse, et al.Pageof 239