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935 related items for PubMed ID: 12210807

  • 1. Spectrum of beta-thalassemia mutations and their association with allelic sequence polymorphisms at the beta-globin gene cluster in an Eastern Indian population.
    Kukreti R, Dash D, E VK, Chakravarty S, Das SK, De M, Talukder G.
    Am J Hematol; 2002 Aug; 70(4):269-77. PubMed ID: 12210807
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  • 2. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
    Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK.
    Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
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  • 4. Molecular analysis of beta-thalassemia in South Vietnam.
    Svasti S, Hieu TM, Munkongdee T, Winichagoon P, Van Be T, Van Binh T, Fucharoen S.
    Am J Hematol; 2002 Oct; 71(2):85-8. PubMed ID: 12353305
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  • 5. Analysis of beta-thalassemia mutations and beta-locus control region hypersensitive sites 2, 3 and 4 in southern Thailand.
    Sriroongrueng W, Schleiemacher E, Panich V, Nopparatana C, Saechan V, Laosombat V, Pornpatkul M, Fukumaki Y.
    Southeast Asian J Trop Med Public Health; 1997 Oct; 28 Suppl 3():120-7. PubMed ID: 9640613
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  • 6. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
    El-Gawhary S, El-Shafie S, Niazi M, Aziz M, El-Beshlawy A.
    Hemoglobin; 2007 Oct; 31(1):63-9. PubMed ID: 17365006
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  • 8. Spectrum of beta thalassemia mutations and HbF levels in the heterozygous Moroccan population.
    Lemsaddek W, Picanço I, Seuanes F, Mahmal L, Benchekroun S, Khattab M, Nogueira P, Osório-Almeida L.
    Am J Hematol; 2003 Jul; 73(3):161-8. PubMed ID: 12827652
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  • 13. Response to hydroxyurea treatment in Iranian transfusion-dependent beta-thalassemia patients.
    Yavarian M, Karimi M, Bakker E, Harteveld CL, Giordano PC.
    Haematologica; 2004 Oct; 89(10):1172-8. PubMed ID: 15477200
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  • 15. combination of IVS2.849 A-G witH IVS1.1 G-A: a mutation of beta-globin gene in a Turkish beta-thalessemia major patient.
    Manguoğlu E, Sargin CF, Nal N, Keser I, Küpesiz A, Yeşilipek A, Lüleci G.
    Pediatr Hematol Oncol; 2005 Jun; 22(4):291-5. PubMed ID: 16020116
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  • 18. Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.
    Bibi A, Messaoud T, Fattoum S.
    Hemoglobin; 2006 Jun; 30(2):175-81. PubMed ID: 16798642
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  • 20. Genotype-phenotype correlation and report of novel mutations in β-globin gene in thalassemia patients.
    Nagar R, Sinha S, Raman R.
    Blood Cells Mol Dis; 2015 Jun; 55(1):10-4. PubMed ID: 25976460
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