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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

89 related items for PubMed ID: 21250884

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  • 2. 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; 39(5):368-70. PubMed ID: 26154945
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  • 4. Homozygous deletion of six olfactory receptor genes in a subset of individuals with Beta-thalassemia.
    Van Ziffle J, Yang W, Chehab FF.
    PLoS One; 2011 Feb 24; 6(2):e17327. PubMed ID: 21390308
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  • 8. A novel (g)gamma(a)gamma(deltabeta)O-thalassemia with a 27 kb deletion.
    Yamashiro Y, Hattori Y, Okayama N, Shinoda E, Suyama N, Tanaka T, Ohi S.
    Hemoglobin; 2005 Feb 24; 29(3):197-208. PubMed ID: 16114183
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  • 12. 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 24; 48(10-11):703-8. PubMed ID: 25866400
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  • 14. Three novel HBB mutations, c.-140C>G (-90 C>G), c.237_256delGGACAACCTCAAGGGCACCT (FS Cd 78/85 -20 bp), and c.315+2T>G (IVS2:2 T>G). Update of the mutational spectrum of β-Thalassemia in Mexican mestizo patients.
    Rizo-de-la-Torre LC, Ibarra B, Sánchez-López JY, Magaña-Torres MT, Rentería-López VM, Perea-Díaz FJ.
    Int J Lab Hematol; 2017 Oct 24; 39(5):539-545. PubMed ID: 28603845
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  • 17. Identification of a novel δ-globin gene mutation in an Iranian family.
    Amirian A, Jafarinejad M, Kordafshari AR, Mosayyebzadeh M, Karimipoor M, Zeinali S.
    Hemoglobin; 2010 Oct 24; 34(6):594-8. PubMed ID: 21077769
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  • 18. Prevalence of -alpha(3.7) and alpha alpha alpha(anti3.7) alleles in sickle cell trait and beta-thalassemia patients in Mexico.
    Nava MP, Ibarra B, Magaña MT, de la Luz Chávez M, Perea FJ.
    Blood Cells Mol Dis; 2006 Oct 24; 36(2):255-8. PubMed ID: 16466950
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