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Journal Abstract Search

200 related items for PubMed ID: 9580456

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  • 44. Molecular and hematological profiles of hemoglobin EE disease with different forms of alpha-thalassemia.
    Fucharoen G, Trithipsombat J, Sirithawee S, Yamsri S, Changtrakul Y, Sanchaisuriya K, Fucharoen S.
    Ann Hematol; 2006 Jul; 85(7):450-4. PubMed ID: 16565831
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  • 48. Erythroid bone marrow activity and red cell hemoglobinization in iron sufficient beta-thalassemia heterozygotes as reflected by soluble transferrin receptor and reticulocyte hemoglobin in content. Correlation with genotypes and Hb A(2) levels.
    Skarmoutsou C, Papassotiriou I, Traeger-Synodinos J, Stamou H, Ladis V, Metaxotou-Mavrommati A, Stamoulakatou A, Kanavakis E.
    Haematologica; 2003 Jun; 88(6):631-6. PubMed ID: 12801838
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  • 49. A report of 8 cases with hemoglobin H disease in an Iranian family.
    Azarkeivan A, Neishabury M, Hadavi V, Esteghamat F, Enrahimkhani S, Najmabadi H.
    Pediatr Hematol Oncol; 2010 Aug; 27(5):405-12. PubMed ID: 20670167
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  • 50. A complex haemoglobinopathy diagnosis in a family with both beta zero- and alpha (zero/+)-thalassaemia homozygosity.
    Giordano PC, Harteveld CL, Bok LA, van Delft P, Batelaan D, Beemer FA, Bernini LF.
    Eur J Hum Genet; 1999 Aug; 7(2):163-8. PubMed ID: 10196699
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  • 52. Hematological phenotypes in children according to the α-globin genotypes.
    Origa R, Barella S, Paglietti ME, Anni F, Danjou F, Denotti AR, Desogus MF, Loi D, Orecchia V, Sollaino MC, Moi P.
    Blood Cells Mol Dis; 2018 Mar; 69():102-106. PubMed ID: 29162392
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  • 54. Evaluation of clinical application of gap-PCR as a routine method for alpha-thalassemia carrier detection.
    Zhou YQ, Xiao GF, Li LY, Li WD, Liu ZY, Zhu LF, Mo QH, Qu XJ, Xu XM.
    Di Yi Jun Yi Da Xue Xue Bao; 2002 May; 22(5):434-6. PubMed ID: 12390707
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  • 56. Fetal hemoglobin and alpha thalassemia modulate the phenotypic expression of HbSD-Punjab.
    Patel DK, Purohit P, Dehury S, Das P, Dutta A, Meher S, Patel S, Bag S, Mashon RS, Das K.
    Int J Lab Hematol; 2014 Aug; 36(4):444-50. PubMed ID: 24245819
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  • 58. An alpha0-thalassemia-like mutation: Hb Suan-Dok [alpha109(G16)Leu-->Arg] carried by a recombinant -alpha(3.7) gene.
    Moradkhani K, Mazurier E, Giordano PC, Wajcman H, Préhu C.
    Hemoglobin; 2008 Aug; 32(4):419-24. PubMed ID: 18654893
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  • 59. Evaluation of a single-tube multiplex polymerase chain reaction screen for detection of common alpha-thalassemia genotypes in a clinical laboratory.
    Bergstrome JA, Poon A.
    Am J Clin Pathol; 2002 Jul; 118(1):18-24. PubMed ID: 12109851
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