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Journal Abstract Search

142 related items for PubMed ID: 2809561

  • 21. Molecular epidemiological study of alpha- and beta-thalassemia in Sihui city.
    Tan JR, Li WJ, Ma JY, Mo QH, Li LY, Jia SQ, Lao XW, Li LY, He RQ, Xu XM.
    Di Yi Jun Yi Da Xue Xue Bao; 2003 Jul; 23(7):716-9. PubMed ID: 12865230
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  • 23. Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?
    Chan LC, Ma SK, Chan AY, Ha SY, Waye JS, Lau YL, Chui DH.
    J Clin Pathol; 2001 Apr; 54(4):317-20. PubMed ID: 11304851
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  • 25. Prenatal prevention for severe thalassemia disease at Srinagarind Hospital.
    Ratanasiri T, Charoenthong C, Komwilaisak R, Changtrakul Y, Fucharoen S, Wongkham J, Kleebkaow P, Seejorn K.
    J Med Assoc Thai; 2006 Oct; 89 Suppl 4():S87-93. PubMed ID: 17725145
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  • 26. The effect of alpha-thalassemia on cord blood red cell indices and interaction with sickle cell gene.
    Quadri MI, Islam SI, Nasserullah Z.
    Ann Saudi Med; 2000 Oct; 20(5-6):367-70. PubMed ID: 17264624
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  • 29. Mean corpuscular volume of heterozygotes for beta-thalassemia correlates with the severity of mutations.
    Rund D, Filon D, Strauss N, Rachmilewitz EA, Oppenheim A.
    Blood; 1992 Jan 01; 79(1):238-43. PubMed ID: 1728311
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  • 31. Prevention and control of thalassemia in Ramathibodi Hospital, Thailand.
    Jaovisidha A, Ajjimarkorn S, Panburana P, Somboonsub O, Herabutya Y, Rungsiprakarn R.
    Southeast Asian J Trop Med Public Health; 2000 Sep 01; 31(3):561-5. PubMed ID: 11289021
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  • 33. Mutational spectrum of thalassemias and other hemoglobinopathies in West Bengal, Eastern India.
    Chatterjee T, Chakravarty A, Chakravarty S.
    Hemoglobin; 2014 Sep 01; 38(6):405-8. PubMed ID: 25405918
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  • 34. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
    Srivorakun H, Fucharoen G, Sae-Ung N, Sanchaisuriya K, Ratanasiri T, Fucharoen S.
    Eur J Haematol; 2009 Jul 01; 83(1):57-65. PubMed ID: 19226360
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  • 35. Erythrocyte indices in a large cohort of β-thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia.
    Singha K, Taweenan W, Fucharoen G, Fucharoen S.
    Int J Lab Hematol; 2019 Aug 01; 41(4):513-518. PubMed ID: 31099487
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  • 37. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS, He J, Zhang J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb 01; 47(2):85-9. PubMed ID: 22455737
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  • 38. Hemoglobin abnormalities. An evaluation on new-born infants and their mothers in a maternity unit close to Brazzaville (P.R. Congo).
    Lallemant M, Galacteros F, Lallemant-Lecoeur S, Feingold J, Carnevale P, Boukila V, Mouchet J, Rosa J.
    Hum Genet; 1986 Sep 01; 74(1):54-8. PubMed ID: 2428730
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  • 39. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct 01; 64(4):1024-32. PubMed ID: 479366
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  • 40. Haematological characteristics of the beta 0 thalassaemia trait in Sardinian children.
    Galanello R, De Virgiliis S, Addis M, Paglietti E, Ruggeri R, Cao A.
    J Clin Pathol; 1980 Oct 01; 33(10):946-8. PubMed ID: 7430359
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