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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

290 related items for PubMed ID: 7267182

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  • 5. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
    Adeyemo T, Ojewunmi O, Oyetunji A.
    Pan Afr Med J; 2014; 18():71. PubMed ID: 25400838
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  • 6. [Analysis of the phenotype-genotype relationship of hemoglobin Q-Thailand in Guangxi].
    Li Y, Chen Z, Liang L, Li R, Liang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):164-8. PubMed ID: 27060306
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  • 7. Beta-cluster haplotypes, alpha-gene status, and hematological data from SS, SC, and S-beta-thalassemia patients in southern California.
    Schroeder WA, Powars DR, Kay LM, Chan LS, Huynh V, Shelton JB, Shelton JR.
    Hemoglobin; 1989 Apr; 13(4):325-53. PubMed ID: 2473969
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  • 14. Hb S, Hb G-Philadelphia and alpha-thalassemia-2 in a Black family.
    Felice AE, Mayson SM, Webber BB, Miller A, Gravely ME, Huisman TH.
    Pediatr Res; 1980 Mar; 14(3):266-7. PubMed ID: 7383748
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  • 16. Screening and diagnosis of Hb Quong Sze [HBA2: c.377T > C (or HBA1)] in a prenatal control program for thalassemia.
    Yang Y, Lou JW, Liu YH, He Y, Li DZ.
    Hemoglobin; 2014 Mar; 38(3):158-60. PubMed ID: 24826791
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  • 17. Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from Georgia.
    Felice AE, McKie KM, Cleek MP, Marino EM, Kutlar A, McKie VC.
    Am J Hematol; 1987 Aug; 25(4):389-400. PubMed ID: 2441597
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  • 20. Hb Westmead (HBA2: c.369C>G): Hematological Characteristics in Heterozygotes with and without α0-Thalassemia.
    Jiang F, Ju AP, Li J, Chen GL, Zhou JY, Tang XW, Zuo LD, Li DZ.
    Hemoglobin; 2020 May; 44(3):153-155. PubMed ID: 32436451
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