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Hemoglobin|July 23, 2014
Incidence of ototoxicity in pediatric patients with transfusion-dependent thalassemia who are less well-chelated by mono- and combined therapy of iron chelating agentsArchwin Tanphaichitr, Thisarat Kusuwan, Siriporn Limviriyakul, et al.Hemoglobin|January 1, 1985
Hematological observations on Arabian SS patients with a homozygosity or heterozygosity for a beta S chromosome with haplotype #31A Kutlar, Y Hattori, I Bakioglu, et al.Hemoglobin|August 6, 2013
Peroxisome proliferator-activated receptor-γ Pro12Ala polymorphism and risk of osteopenia in β-thalassemia major patientsMehdi Sahmani, Abdollah Gholami, Azita Azarkeivan, et al.Hemoglobin|August 7, 2013
The spectrum of β-thalassemia mutations in Kermanshah Province in West Iran and its association with hematological parametersMasomeh Mehrabi, Reza Alibakhshi, Soheila Fathollahi, et al.Hemoglobin|December 30, 2015
β-Thalassemia Haplotypes in Romania in the Context of Genetic Mixing in the Mediterranean AreaLaudy Cherry, Carla Calo, Rodica Talmaci, et al.Hemoglobin|January 13, 2016
The Codon 35 (A > G) (HBB: c.107A > G) at the α-β Chain Interface of the β-Globin Gene: A Silent Mutation?Man-Yu Wu, Dong-Zhi LiHemoglobin|February 7, 2016
First Report of a Dominantly Inherited β-Thalassemia Caused by a Novel Elongated β-Globin ChainSamaneh Farashi, Fariba Rad, Bahram Shahmohammadi, et al.Hemoglobin|February 26, 2016
A New Intergenic α-Globin Deletion (α-αΔ125) Found in a Kabyle PopulationAmrathlal Rabbind Singh, Philippe Lacan, Estelle Cadet, et al.Hemoglobin|January 1, 1989
Characterization of beta-thalassemia mutations among the JapaneseY Hattori, A Yamane, Y Yamashiro, et al.Hemoglobin|September 3, 2015
Mutations on the α2-Globin Gene That May Trigger α(+)-ThalassemiaSamaneh Farashi, Shadi Vakili, Negin F Garous, et al.Pageof 238