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Journal Abstract Search

152 related items for PubMed ID: 11189500

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  • 27. [Study on the incidence of beta-Thalassemia and genotypes among children under 7 year-olds in Nanning, Liuzhou and Baise areas, Guangxi province].
    Qiu XQ, Chen P, Zhang N, Zeng XY, Huang CQ, Chen WQ, Lin WX, Li SQ.
    Zhonghua Liu Xing Bing Xue Za Zhi; 2009 Oct; 30(10):1021-4. PubMed ID: 20193381
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  • 28. [Diagnostic strategy of beta-thalassemic mutation in a Tunisian family, application in prenatal diagnosis].
    Khelil AH, Laradi S, Ferchichi S, Carion N, Béjaoui M, Saad A, Chaieb A, Miled A, Ben Chibani J, Perrin P.
    Ann Biol Clin (Paris); 2003 Oct; 61(2):229-33. PubMed ID: 12702481
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  • 29. 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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  • 30. [Cell-free fetal DNA detection in maternal plasma using real-time PCR and cycling probe technology for prenatal screening beta-thalassaemia major].
    Chen X, Ren JH, Guo H, Lin LH, Yao QX.
    Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jul; 28(7):1210-3. PubMed ID: 18676265
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  • 32. 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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  • 33. [Screening of beta zero-thalassemia in cord blood from 2,423 newborns in Xilin county of Guangxi].
    Pan H, Li Q, Zhao G.
    Zhonghua Xue Ye Xue Za Zhi; 1999 Oct; 20(10):527-8. PubMed ID: 11721399
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  • 35. Hemoglobin D/beta-thalassemia and beta-thalassemia major in a Saudi family.
    Owaidah TM, Al-Saleh MM, Al-Hellani AM.
    Saudi Med J; 2005 Apr; 26(4):674-7. PubMed ID: 15900384
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  • 36. High-throughput beta-thalassemia carrier screening by allele-specific Q-primer real-time polymerase chain reaction.
    Liu X, Law HY, Tan YM, Hong Y.
    Anal Biochem; 2010 Sep 01; 404(1):97-9. PubMed ID: 20433808
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  • 37. [A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].
    Li Q, Li LY, Mo QH.
    Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jan 01; 28(1):16-9. PubMed ID: 18227017
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  • 38. Observation of a rare hemoglobin variant [Hb Lulu island, beta107(G9)Gly-->Asp, GGC-->GAC] co-inherited with a beta+-thalassemia mutation [IVS-I-110 (G-->A)] or in the heterozygous state in a Greek-Albanian family.
    Papassotiriou I, Stamoulakatou A, Wajcman H, Kister J, Dimisianos G, Lazaropoulou C, Kanavaki I, Vavourakis E, Kattamis A, Kanavakis E, Traeger-Synodinos J.
    Hemoglobin; 2006 Jan 01; 30(4):409-18. PubMed ID: 16987796
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  • 39. A new genotyping method for detecting low abundance single nucleotide mutations based on gap ligase chain reaction and quantitative PCR assay.
    Yi P, Jiang H, Li L, Dai F, Zheng Y, Han J, Chen Z, Guo J.
    Cell Biochem Biophys; 2012 Jan 01; 62(1):161-7. PubMed ID: 22006255
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  • 40. Identification of a novel frameshift mutation at codon 53 (-T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao family.
    Yi P, Yu F, Huang S, Zhong C, Li Q, Yang Y, Zhang W, Xiao C, Xu X.
    Blood Cells Mol Dis; 2008 Jan 01; 41(1):56-9. PubMed ID: 18381244
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