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Hemoglobin|November 15, 2011
Use of hormone replacement therapy for correction of high turnover bone disease in hypogonadal β-Thalassemia major patients presenting with osteoporosis: comparison with idiopathic premature ovarian failureRatna Chatterjee, Maurice Katz, Rekha BajoriaHemoglobin|January 1, 1995
Molecular basis of alpha-thalassemia in PortugalM J Peres, L Romão, H Carreiro, et al.Hemoglobin|February 1, 1993
Beta-thalassemia mutations in the Portuguese; high frequencies of two alleles in restricted populationsG P Tamagnini, P Gonçalves, M L Ribeiro, et al.Hemoglobin|August 1, 1996
The relative levels of different types of beta-mRNA and beta-globin in BFU-E derived colonies from patients with beta chain variants; further evidence for somatic mosaicism in the Hb Costa Rica carrier [beta 77(EF1)His-->Arg]N S Smetanina, L H Gu, W E Rodriguez Romero, et al.Hemoglobin|January 1, 1997
Detection of the alpha-thalassemia-2 (3.7 kb) deletion in DNA extracted from 20-year-old blood smearsJ E Okeagu, N S Smetanina, T H HuismanHemoglobin|January 1, 1977
Effect of 2, 3-diphosphoglycerate on the solubility of deoxy-sickle hemoglobinP H Swerdlow, R A Bryan, J F Bertles, et al.Hemoglobin|January 1, 1977
An improved chromatographic procedure for quantitation of human fetal hemoglobinE C Abraham, A Reese, M Stallings, et al.Hemoglobin|January 1, 1977
Binding of Protoporphyrin to hemoglobin in red blood cells of patients with erythropoietic protoporphyriaJ van Steveninck, T M Dubbelman, A F de Goeij, et al.Hemoglobin|November 9, 2016
A Patient with β-Thalassemia Intermedia Secondary to Homozygosity for a Polyadenylation Signal Mutation (AATAAA > AATAGA) (HBB: C.*112A > G) on the β-Globin GeneYen-Chian Lim, Karen M L Tan, Samuel S Chong, et al.Pageof 238