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Journal Abstract Search

212 related items for PubMed ID: 35168445

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  • 4. Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in Cis.
    Colaco S, Trivedi A, Colah RB, Ghosh K, Nadkarni AH.
    Hemoglobin; 2014; 38(1):24-7. PubMed ID: 24200152
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  • 5. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
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  • 6. δ-Thalassemia with Complete Absence of Hb A2 in a Chinese Family.
    Tang HS, Wang DG, Huang LY, Li DZ.
    Hemoglobin; 2018 Mar; 42(2):135-137. PubMed ID: 29737888
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  • 8. A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)].
    Yan JM, Zhou JY, Xie XM, Li J, Li DZ.
    Hemoglobin; 2016 Jun; 40(3):213-4. PubMed ID: 27117573
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  • 9. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
    Moassas F, Nweder MS, Murad H.
    BMC Pediatr; 2019 Feb 18; 19(1):61. PubMed ID: 30777047
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  • 17. Analysis of δ-globin gene mutations in the Chinese population.
    Liu N, Xie XM, Zhou JY, Li R, Liao C, Li DZ.
    Hemoglobin; 2013 Feb 18; 37(1):85-93. PubMed ID: 23215833
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  • 20. A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A].
    Moumni I, Zorai A, Mahjoub S, Mosbahi I, Chaouechi D, Benromdhane N, Abbes S.
    Hemoglobin; 2014 Feb 18; 38(2):88-90. PubMed ID: 24471655
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