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Hemoglobin|January 1, 1977
Some properties of hemoglobin Gun HillJ Murari, L L Smith, J B Wilson, et al.Hemoglobin|January 1, 1977
A test tube method for quantitation of hemoglobin A2 using DE 52 celluloseD Nastev, G D Efremov, G PetkovHemoglobin|February 12, 2009
Diversity of the 5' beta-globin haplotype of four beta-thalassemia mutations in the Mexican populationKarina R Morales, Maria T Magaña, Bertha Ibarra, et al.Hemoglobin|February 12, 2009
Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG)Barry Eng, Lynda Walker, John S WayeHemoglobin|July 26, 2008
Hb Montreal II: a novel elongated beta-globin variant caused by a frameshift mutation [beta142 (-C)]Pierre Chagnon, Luigina Mollica, Claude Belisle, et al.Hemoglobin|July 26, 2008
First observation of Hb Taybe [Codons 38/39 (-Acc) Thr-->0 (alpha1)] in Greece: clinical and hematological findings in patients with co-inherited alpha+-thalassemia mutationsVarvara Douna, Dimitra Liapi, Dimitrios Kampourakis, et al.Hemoglobin|July 26, 2008
Further identification of the hyperunstable alpha-globin chain variant Hb Heraklion [codons 36/37 (-CCC); Pro-->0 (alpha1)] in Greek cases with co-inherited alpha+-thalassemia mutationsVarvara Douna, Ioannis Papassotiriou, Anna Metaxotou-Mavrommati, et al.Hemoglobin|July 26, 2008
An unusually frequent beta-thalassemia mutation in an Iranian ProvincePeyman Eshghi, Azita Zadeh-Vakili, Armin Rashidi, et al.Hemoglobin|August 25, 2005
A rare association of alphaO-thalassemia (--SEA) and an initiation codon mutation (ATG-->A-G) of the alpha2 gene causes Hb H disease in ThailandVip Viprakasit, Worrawut Chinchang, Waraporn Glomglao, et al.Hemoglobin|August 24, 2005
Clinical and laboratory effects of hydroxyurea in children and adolescents with sickle cell anemia: a Portuguese hospital studyLígia Barbosa Braga, Ana Cristina Ferreira, Margarida Guimarães, et al.Pageof 239