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PUBMED FOR HANDHELDS

Journal Abstract Search

247 related items for PubMed ID: 23586372

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  • 2. Molecular heterogeneity of beta-thalassemia alleles in Spain and its importance in the diagnosis and prevention of beta-thalassemia major and sickle cell disorders.
    Pereira Mdel M, Dalmau AC, Corrons JL.
    Hemoglobin; 2009; 33(3):226-34. PubMed ID: 19657837
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  • 3. Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A2 Levels.
    Satthakarn S, Panyasai S, Pornprasert S.
    Hemoglobin; 2020 Sep; 44(5):349-353. PubMed ID: 33023363
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  • 4. Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia.
    Vinciguerra M, Passarello C, Cassarà F, Leto F, Cannata M, Calvaruso G, Di Maggio R, Renda D, Maggio A, Giambona A.
    Int J Lab Hematol; 2016 Feb; 38(1):17-26. PubMed ID: 26418075
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  • 5. Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients.
    Azarkeivan A, Cohan N, Niazkar HR, Azizi A, Rad F.
    Hemoglobin; 2020 Mar; 44(2):109-112. PubMed ID: 32370567
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  • 6. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene.
    Panyasai S, Jaiping K, Pornprasert S.
    Hemoglobin; 2015 Mar; 39(4):292-5. PubMed ID: 26029792
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  • 7. Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotype.
    Daniel Y, Hill K, Inusa B, Thein SL, Howard J.
    Hemoglobin; 2011 Mar; 35(4):406-10. PubMed ID: 21797706
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  • 13. Coinheritance of Hb S [β6(A3)Glu→Val, GAG>GTG] with β0-thalassemia codon 17 (A>T) in a Thai patient.
    Pornprasert S, Panyasai S, Kongthai K, Treesuwan K.
    Hemoglobin; 2012 Mar; 36(3):265-9. PubMed ID: 22471390
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  • 14. Prenatal diagnosis of sickle cell anemia and beta-thalassemia in southern Turkey.
    Cürük MA, Zeren F, Genç A, Ozavci-Aygün S, Kilinç Y, Aksoy K.
    Hemoglobin; 2008 Mar; 32(6):525-30. PubMed ID: 19065329
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  • 16. Clinical to Molecular Screening Paradigm for β-Thalassemia Carriers.
    Abdel-Messih IY, Youssef SR, Mokhtar GM, Elmogy MI, Mahmoud HM, Ayoub M, Pessar SA.
    Hemoglobin; 2015 Mar; 39(4):240-6. PubMed ID: 26076393
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  • 17. Splice Acceptor Mutation [HBB:c.93-2A > T] in a Patient with Hb S/β0-Thalassemia.
    Waye JS, Hanna M, Nakamura L, Walker L, Eng B, Nfonsam LE.
    Hemoglobin; 2024 Mar; 48(2):116-117. PubMed ID: 38360540
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  • 20. First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family.
    Murad H, Moassas F.
    Hemoglobin; 2019 Jan; 43(1):66-68. PubMed ID: 30843739
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