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Journal Abstract Search

181 related items for PubMed ID: 23577918

  • 1. Application of multiplex ligation-dependent probe amplification to screen for β-globin cluster deletions: detection of two novel deletions in a multi ethnic population.
    Cui J, Azimi M, Baysdorfer C, Vichinsky EP, Hoppe CC.
    Hemoglobin; 2013; 37(3):241-56. PubMed ID: 23577918
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  • 2. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
    Esteghamat F, Imanian H, Azarkeivan A, Pourfarzad F, Almadani N, Najmabadi H.
    Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
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  • 3. A single-tube multiplex gap-polymerase chain reaction for the detection of eight β-globin gene cluster deletions common in Southeast Asia.
    Tritipsombut J, Phylipsen M, Viprakasit V, Chalaow N, Sanchaisuriya K, Giordano PC, Fucharoen S, Harteveld CL.
    Hemoglobin; 2012; 36(6):571-80. PubMed ID: 23181748
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  • 4. Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH.
    Blattner A, Brunner-Agten S, Ludin K, Hergersberg M, Herklotz R, Huber AR, Röthlisberger B.
    Blood Cells Mol Dis; 2013 Jun; 51(1):39-47. PubMed ID: 23491071
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  • 5. Genetic research and clinical analysis of β-globin gene cluster deletions in the Chinese population of Fujian province: A 14-year single-center experience.
    Chen M, Zhang M, Chen L, Lin N, Wang Y, Xu L, Huang H.
    J Clin Lab Anal; 2022 Feb; 36(2):e24181. PubMed ID: 34951062
    [Abstract] [Full Text] [Related]

  • 6. Identification and molecular characterization of a novel 55-kb deletion recurrent in southern Italy: the Italian (G) γ((A) γδβ)°-thalassemia.
    Lacerra G, Prezioso R, Musollino G, Piluso G, Mastrullo L, De Angioletti M.
    Eur J Haematol; 2013 Mar; 90(3):214-9. PubMed ID: 23281611
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  • 7. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.
    Prakobkaew N, Fucharoen S, Fuchareon G, Siriratmanawong N.
    Eur J Haematol; 2014 Jan; 92(1):73-9. PubMed ID: 24112054
    [Abstract] [Full Text] [Related]

  • 8. Detection and characterisation of beta-globin gene cluster deletions in Chinese using multiplex ligation-dependent probe amplification.
    So CC, So AC, Chan AY, Tsang ST, Ma ES, Chan LC.
    J Clin Pathol; 2009 Dec; 62(12):1107-11. PubMed ID: 19946097
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  • 13. A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization.
    Singha K, Fucharoen G, Hama A, Fucharoen S.
    Clin Biochem; 2015 Jul; 48(10-11):703-8. PubMed ID: 25866400
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  • 14. Screening for common β-globin gene cluster deletions in Chinese individuals with increased hemoglobin F.
    Cai WJ, Li J, Xie XM, Li DZ.
    Int J Lab Hematol; 2015 Dec; 37(6):752-7. PubMed ID: 26179971
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  • 15. Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion.
    Waye JS, Eng B, Got T, Hanna M, Hohenadel BA, Nakamura LM, Walker L.
    Hemoglobin; 2015 Dec; 39(5):368-70. PubMed ID: 26154945
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  • 16. Identification and molecular characterization of four new large deletions in the beta-globin gene cluster.
    Joly P, Lacan P, Garcia C, Couprie N, Francina A.
    Blood Cells Mol Dis; 2009 Dec; 43(1):53-7. PubMed ID: 19269866
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  • 17. Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.
    Fornari TA, Lanaro C, Albuquerque DM, Ferreira R, Costa FF.
    Exp Biol Med (Maywood); 2017 Feb; 242(3):267-274. PubMed ID: 27591578
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  • 20. The prevalence and molecular characterization of (δβ)0 -thalassemia and hereditary persistence of fetal hemoglobin in the Chinese Zhuang population.
    He S, Wei Y, Lin L, Chen Q, Yi S, Zuo Y, Wei H, Zheng C, Chen B, Qiu X.
    J Clin Lab Anal; 2018 Mar; 32(3):. PubMed ID: 28763119
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