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Journal Abstract Search


121 related items for PubMed ID: 27117572

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  • 2. Compound Heterozygosity for Hb D-Ibadan (HBB: c.263C>A) and Hb C (HBB: c.19G>A).
    Kundrapu S, Janaki N, Meyerson HJ.
    Hemoglobin; 2018 Jul; 42(4):269-271. PubMed ID: 30604644
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  • 6. Compound Heterozygosity for Hb Alperton (HBB: c.407C>T) and IVS-I-5 (G>C) (HBB: c.92+5G>C) Mutations Presenting as a Moderate Anemia in an Indian Family.
    Godbole KG, Ramachandran A, Karkamkar AS, Dalal AB.
    Hemoglobin; 2018 Mar; 42(2):141-142. PubMed ID: 29651865
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  • 7. Severe Drug-Induced Hemolysis in a Patient with Compound Heterozygosity for Hb Peterborough (HBB: c.334G>T) and Hb Lepore-Boston-Washington (NG_000007.3: g.63632_71046del).
    Agbuduwe C, Rugless M, Asba N, Proven M, Sivakumaran M.
    Hemoglobin; 2019 Jan; 43(1):56-59. PubMed ID: 31060398
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  • 8. Compound heterozygosity for hemoglobin C and Korle-Bu: moderate microcytic hemolytic anemia and acceleration of crystal formation [corrected].
    Nagel RL, Lin MJ, Witkowska HE, Fabry ME, Bestak M, Hirsch RE.
    Blood; 1993 Sep 15; 82(6):1907-12. PubMed ID: 7691242
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  • 10. Compound heterozygosity for Hb Spanish town [alpha27(B8)Glu-->Val], Hb S [beta6(A3)Glu-->Val] and the -alpha(3.7kb) thalassemia deletion.
    Faustino P, Picanço I, Miranda A, Seixas T, Ferrão A, Morais A, Lavinha J, Romão L.
    Hemoglobin; 2002 May 15; 26(2):185-9. PubMed ID: 12144063
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  • 11. Compound heterozygosity for Hb Lepore-Boston and Hb Neapolis (Dhonburi) [beta 126(H4)Val-->Gly] in a patient from Naples, Italy.
    Pagano L, Carbone V, Fioretti G, Viola A, Buffardi S, Rametta V, Desicato S, Pucci P, De Rosa C.
    Hemoglobin; 1997 Jan 15; 21(1):1-15. PubMed ID: 9028819
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  • 13. [Hematological Analysis and Diagnosis of Two Rare Abnormal Hemoglobin].
    Wang JC, Guo H, Huang HJ, Yuan TL, Yao CZ, Qin DQ, DU L.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2020 Dec 15; 28(6):2028-2032. PubMed ID: 33283737
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  • 14. Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis.
    Girisha KM, Vahab SA, Dalal AB, Gopinath PM, Satyamoorthy K.
    Ann Hematol; 2010 Jun 15; 89(6):625-6. PubMed ID: 19727721
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  • 15. Homozygosity for HBA1: c.179G > A: Hb Adana in an infant.
    Aksu T, Yarali N, Bayram C, Fettah A, Avci Z, Tunç B.
    Hemoglobin; 2014 Jun 15; 38(6):449-50. PubMed ID: 25342395
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  • 17. Hb Osu-Christiansborg [beta52(D3)Asp --> Asn]: a de novo mutation in Brazil.
    Rodrigues de Souza L, Kimura EM, Albuquerque DM, Costa FF, de Fátima Sonati M.
    Hemoglobin; 2004 Feb 15; 28(1):65-8. PubMed ID: 15008267
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  • 18. Hemoglobin C--G-Georgia double heterozygosity: a case report.
    Reynolds S, Miller C, King R, Lazarchick J.
    Ann Clin Lab Sci; 1992 Feb 15; 22(6):414-6. PubMed ID: 1456731
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  • 19. Anthropometric data of children heterozygous for abnormal hemoglobins (Hb AS, Hb AC) and paired controls Hb AA.
    Freire-Maia N, Paes Alves AF, Oliveira MP, Olympio da Silva MC, Lima Machado MA, Azevêdo ES.
    Hum Hered; 1981 Feb 15; 31(2):70-3. PubMed ID: 7228060
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