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Hemoglobin|June 9, 2004
Beta-globin gene cluster haplotypes linked to the betaS gene in western IndiaMalay B Mukherjee, Reema R Surve, Raman R Gangakhedkar, et al.Hemoglobin|January 1, 1992
A new variant, HB Muscat [alpha 2 beta (2)32(B14)Leu----Val] observed in association with HB S in an Arabian familyM Ramachandran, L H Gu, J B Wilson, et al.Hemoglobin|January 1, 1992
Hb Bab-Saadoun or alpha 2 beta (2)48(CD7)Leu----Pro, a mildly unstable variant found in an Arabian boy from TunisiaT P Molchanova, J B Wilson, L H Gu, et al.Hemoglobin|March 11, 2004
Diagnosis and characterization of Hb C/Hb Iowa: a rare but easily misidentified compound heterozygous conditionSaika Somjee, Lolie C Yu, Arthur F Hagar, et al.Hemoglobin|June 22, 2017
Population-Based Genetic Study of β-Thalassemia Mutations in Mardan Division, Khyber Pakhtunkhwa Province, PakistanRaj Muhammad, Muhammad Shakeel, Shoaib U Rehman, et al.Hemoglobin|June 16, 2017
The Assessment of Skin Color and Iron Levels in Pediatric Patients with β-Thalassemia Major Using a Visual Skin Color ChartIbrahim H Bucak, Habip Almis, Samet Benli, et al.Hemoglobin|July 24, 2018
Molecular Spectrum of α- and β-Thalassemia Mutations in a Large Ethnic Hakka Population in Southern ChinaPingsen Zhao, Ruiqiang Weng, Heming WuHemoglobin|January 1, 1990
Hb Hekinan observed in three Chinese from Macau; identification of the GAG----GAT mutation in the alpha 1-globin geneW Zhao, J B Wilson, B B Webber, et al.Hemoglobin|April 11, 2018
Left Ventricular Diastolic Dysfunction in β-Thalassemia Major with Heart FailureLuigi Mancuso, Angela Vitrano, Andrea Mancuso, et al.Hemoglobin|May 9, 2018
δ-Thalassemia with Complete Absence of Hb A<sub>2</sub> in a Chinese FamilyHai-Shen Tang, De-Gang Wang, Lv-Yin Huang, et al.Pageof 238