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Hemoglobin|March 10, 2017
β-Thalassemia gene mutations in Antalya, Turkey: results from a single centre studyAyşegül Kurtoğlu, Volkan Karakuş, Özgür Erkal, et al.
Hemoglobin|January 1, 1989
Hb Moriguchi or alpha 2 beta 2(97) (FG4)His---Tyr substitution at the alpha 1-beta 2 interfaceY Ohba, K Imai, I Kumada, et al.
Hemoglobin|November 11, 2016
A novel compound heterozygosity in Southern China: IVS-II-5 (G > C) and IVS-II-672 (A > C)Lin Zhao, Jilin Qing, Yue Liang, et al.
Hemoglobin|October 1, 2016
Can Neuroimaging Markers of Vascular Pathology Explain Cognitive Performance in Adults With Sickle Cell Anemia? A review of the LiteratureDana R Jorgensen, Caterina Rosano, Enrico M Novelli
Hemoglobin|October 1, 2016
Molecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern IranSima M Derakhshan, Mahmoud S Khaniani, Fateme Afkhami, et al.
Hemoglobin|August 12, 2003
Hb Bronte or alpha93(FG5)Val-->Gly: a new unstable variant of the alpha2-globin gene, associated with a mild alpha(+)-thalassemia phenotypeGiuseppina Lacerra, Rosario Testa, Maria De Angioletti, et al.
Hemoglobin|August 12, 2003
Molecular characterization of alpha-thalassemia in PakistanShaheen N Khan, Farrukh Hasan, Carla Sollaino, et al.
Hemoglobin|March 11, 2004
Detection of rare beta-thalassemia mutations by denaturing gradient gel electrophoresis among IndiansAjit C Gorakshakar, Supriya P Phanasgaonkar, Anita H Nadkarni, et al.
Hemoglobin|March 11, 2004
The beta-thalassemia mutation/haplotype distribution in the moroccan populationWafaâ Lemsaddek, Isabel Picanço, Filomena Seuanes, et al.
Hemoglobin|January 1, 1992
Clinical, hematological, and molecular features in Sicilians with sickle cell diseaseG Schilirò, P Samperi, C Consalvo, et al.
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