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Journal Abstract Search

207 related items for PubMed ID: 31450984

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  • 4. First description of a Hb A2 variant in Thailand. Identification of Hb A2-Melbourne [δ43(CD2)Glu→Lys] in Thai individuals.
    Chaibunruang A, Fucharoen G, Fucharoen S.
    Hemoglobin; 2012; 36(1):80-4. PubMed ID: 21967556
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  • 5. Detection of a Hb A2 -Melbourne (HBD: c.130G>A) combined with β-thalassemia in a Chinese individual.
    Li Y, Huang T, Mao T, Zhang X, Liang L, Meng M.
    J Clin Lab Anal; 2020 Sep; 34(9):e23401. PubMed ID: 32770585
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  • 6. Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn, HBB: c.[79G>A;198G>C]): A Novel β-Thalassemic Hemoglobin Variant.
    Satthakarn S, Boonmee S, Panyasai S.
    Hemoglobin; 2020 Nov; 44(6):385-390. PubMed ID: 33222574
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  • 7. Phenotypic Expression of Known and Novel Hemoglobin A2-Variants, Hemoglobin A2-Mae Phrik [Delta 52(D3) Asp > Gly, HBD:c.158A > G], Associated with Hemoglobin E [Beta 26(B8) Glu > Lys, HBB:c.79G > A] in Thailand.
    Phasit A, Panyasai S, Mayoon M, Jettawan N, Satthakarn S.
    Genes (Basel); 2022 May 27; 13(6):. PubMed ID: 35741722
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  • 8. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.
    Eur J Haematol; 2007 Nov 27; 79(5):422-8. PubMed ID: 17916081
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  • 9. Micromapping of thalassemia and hemoglobinopathies in diferent regions of northeast Thailand and Vientiane, Laos People's Democratic Republic.
    Tritipsombut J, Sanchaisuriya K, Phollarp P, Bouakhasith D, Sanchaisuriya P, Fucharoen G, Fucharoen S, Schelp FP.
    Hemoglobin; 2012 Nov 27; 36(1):47-56. PubMed ID: 22122810
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  • 10. Hb Agenogi [β90(F6)Glu→Lys (GAG>AAG) HBB: c.271G>A)] in a Pregnant Thai Woman.
    Panyasai S, Thongsuk P, Pornprasert S.
    Hemoglobin; 2016 Nov 27; 40(2):134-7. PubMed ID: 26864977
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  • 11. Known and new hemoglobin A2 variants in Thailand and implication for β-thalassemia screening.
    Panyasai S, Fucharoen G, Fucharoen S.
    Clin Chim Acta; 2015 Jan 01; 438():226-30. PubMed ID: 25218786
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  • 12. Complex Interaction of Hb Q-Thailand (HBA1: c.223G>C) with β-Thalassemia/Hb E (HBB: c.79G>A) Disease.
    Panyasai S, Satthakarn S, Pornprasert S.
    Hemoglobin; 2018 Jan 01; 42(1):54-57. PubMed ID: 29484903
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  • 13. Hemoglobin profile and molecular characteristics of the complex interaction of hemoglobin Doi-Saket [α9(A7) asn > lys, HBA2:c.30C > a], a novel α2α1 hybrid globin variant, with hemoglobin E [β26(B8) Glu > lys, HBB:c.79G > A] and deletional α+-thalassemia in a Thai family.
    Panyasai S, Khongthai K, Satthakarn S.
    Ann Med; 2023 Jan 01; 55(2):2264174. PubMed ID: 37796611
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  • 15. β-Hemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program.
    Singha K, Chaibunruang A, Souvanlasy B, Srivorakun H, Yamsri S, Fucharoen G, Fucharoen S.
    Int J Lab Hematol; 2021 Jun 01; 43(3):500-505. PubMed ID: 33244864
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  • 16. Molecular Characteristics of Hb New York [β113(G15)Val→Glu, HBB: c.341T>A] in Thailand.
    Chaibunruang A, Singha K, Srivorakun H, Fucharoen G, Fucharoen S.
    Hemoglobin; 2018 Jan 01; 42(1):11-15. PubMed ID: 29464999
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  • 20. 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 01; 38(2):88-90. PubMed ID: 24471655
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