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Journal Abstract Search

481 related items for PubMed ID: 18932077

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  • 5. Detection of Hb Constant Spring [α142, Term→Gln, TAA>CAA (α2)] in heterozygotes combined with β-thalassemia.
    Li YQ, Li R, Li DZ.
    Hemoglobin; 2013; 37(2):197-200. PubMed ID: 23390935
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  • 7. 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 mutation.
    Moumni I, Zorai A, Daoued BB, Mosbahi I, Omar S, Kaabachi N, Dellagi K, Abbes S.
    Hemoglobin; 2007; 31(1):23-9. PubMed ID: 17365002
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  • 8. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy.
    Sanchaisuriya K, Chunpanich S, Fucharoen S, Fucharoen G, Sanchaisuriya P, Changtrakun Y.
    Eur J Haematol; 2005 Mar; 74(3):221-7. PubMed ID: 15693792
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  • 12. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.
    Azma RZ, Othman A, Azman N, Alauddin H, Ithnin A, Yusof N, Razak NF, Sardi NH, Hussin NH.
    Malays J Pathol; 2012 Jun; 34(1):57-62. PubMed ID: 22870600
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  • 13. A Novel Mutation of the α2-Globin Gene Causing α+-Thalassemia: Hb Nanning (HBA2: c.369_370delinsGA).
    Chen B, Lin L, Yi S, Chen Q, Wei H, Li G, Zheng C, He S, Qiu X.
    Hemoglobin; 2017 Jan; 41(1):56-58. PubMed ID: 28395547
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  • 14. A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A].
    Moumni I, Zorai A, Mahjoub S, Mosbahi I, Chaouechi D, Benromdhane N, Abbes S.
    Hemoglobin; 2014 Jan; 38(2):88-90. PubMed ID: 24471655
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  • 15. Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in Cis.
    Colaco S, Trivedi A, Colah RB, Ghosh K, Nadkarni AH.
    Hemoglobin; 2014 Jan; 38(1):24-7. PubMed ID: 24200152
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  • 16. Delta-thalassemia in Cyprus.
    Pavlou E, Phylactides M, Kyrri A, Kalogerou E, Makariou C, Georgiou I, Kleanthous M.
    Hemoglobin; 2006 Jan; 30(4):455-62. PubMed ID: 16987800
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  • 20. Two new delta-globin mutations: Hb A2-Ninive [delta133(H11)Val-Ala] and a delta(+)-thalassemia mutation [-31 (A --> G)] in the TATA box of the delta-globin gene.
    Frischknecht H, Dutly F.
    Hemoglobin; 2005 Jan; 29(2):151-4. PubMed ID: 15921167
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