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Hb M Dothan [beta 25/26 (B7/B8)/(GGT/GAG-->GAG//Gly/Glu-->Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics.

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Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.

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Precision Medicine in Transfusion-Dependent and Non-Transfusion-Dependent β-Thalassemia: Toward Personalized Diagnosis and Therapy.

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Compound Heterozygosity for Hb Port Phillip and the -α3.7 Deletion Leads to Persistent Hypoxemia in a Chinese Pediatric Family.

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Annals of medicine and surgery (2012)·2026

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Hb Gainesville-GA or alpha 2 beta 2(46)(CD5)Gly----Arg; second report

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