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Hemoglobin|September 28, 2017
Rivaroxaban Use in Patients with HemoglobinopathiesChrysoula Apostolou, Philippos Klonizakis, Maria Mainou, et al.Hemoglobin|January 8, 2019
First Identification of the 3.5 kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the β-Globin Gene Cluster in a Chinese FamilySheng He, Qian Qin, Li Lin, et al.Hemoglobin|January 11, 2019
Rare Association of Hb D-Los Angeles (HBB: c.364G>C) with Hb H Disease: Diagnosis and Clinical ImplicationsAikaterini Zioga, Eleni Thanopoulou, Elissavet Hatzi, et al.Hemoglobin|January 11, 2019
Rare β- and δ-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, IndiaAjit C Gorakshakar, Pearl V Breganza, Stacy P Colaco, et al.Hemoglobin|March 17, 2007
Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutationImen Moumni, Amine Zorai, Bechir Ben Daoued, et al.Hemoglobin|March 17, 2007
Misdiagnosis of Hb constant spring (alpha142, Term-->Gln, TAA-->CAA in alpha2) in a Hb H (beta4) disease childDongzhi Li, Can Liao, Jian LiHemoglobin|January 1, 1991
Sickle cell anemia in the Tunisian population: haplotyping and HB F expressionS Abbes, S Fattoum, M Vidaud, et al.Hemoglobin|July 27, 2007
The molecular analysis of beta-thalassemia mutations in Lorestan Province, IranAli Asghar Kiani, Yousef Mortazavi, Sirous Zeinali, et al.Hemoglobin|September 22, 2006
The prevalence and molecular basis of hemoglobinopathies in CambodiaBenedict P Carnley, John F Prior, Anne Gilbert, et al.Hemoglobin|June 27, 2006
Hb Marineo [beta70(E14)Ala-->Val]: a silent hemoglobin variant with a mutation within the heme pocketAntonino Giambona, Margherita Vinciguerra, Filippo Cassarà, et al.Pageof 240