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Journal Abstract Search

2185 related items for PubMed ID: 17916081

  • 1. 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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  • 2. Delta-thalassemia in Cyprus.
    Pavlou E, Phylactides M, Kyrri A, Kalogerou E, Makariou C, Georgiou I, Kleanthous M.
    Hemoglobin; 2006 Nov; 30(4):455-62. PubMed ID: 16987800
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  • 3. Known and new delta globin gene mutations and their diagnostic significance.
    Bouva MJ, Harteveld CL, van Delft P, Giordano PC.
    Haematologica; 2006 Jan; 91(1):129-32. PubMed ID: 16434382
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  • 4. Molecular evidences of single mutational events followed by recurrent crossing-overs in the common delta-globin alleles in the Mediterranean area.
    Lacerra G, Musollino G, Scarano C, Lagona LF, Caruso DG, Testa R, Prezioso R, Di Noce F, Medulla E, Friscia MG, Mastrullo L, Caldora M, Nota L, Gaudiano C, Magnano C, Ciaccio C, Romeo MA, Carestia C.
    Gene; 2008 Feb 29; 410(1):129-38. PubMed ID: 18221842
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  • 5. HbA2-Partinico or delta(A2)Pro-->Thr, a new genetic variation in the delta-globin gene in cis to the beta(+) thal IVS-I-110 G>A, and the heterogeneity of delta-globin alleles in double heterozygotes for beta- and delta-globin gene defects.
    Lacerra G, Scarano C, Musollino G, Testa R, Prezioso R, Caruso DG, Lagona LF, Medulla E, Friscia MG, Gaudiano C, Carestia C.
    Ann Hematol; 2010 Feb 29; 89(2):127-34. PubMed ID: 19609526
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  • 6. Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features.
    De Angioletti M, Lacerra G, Gaudiano C, Mastrolonardo G, Pagano L, Mastrullo L, Masciandaro S, Carestia C.
    Hum Mutat; 2002 Nov 29; 20(5):358-67. PubMed ID: 12402333
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  • 11. A study of δ-globin gene mutations in the UK population: identification of three novel variants and development of a novel DNA test for Hb A'2.
    Khalil MS, Marouf S, Element D, Timbs A, Gallienne A, Schuh A, Old JM, Henderson S.
    Hemoglobin; 2014 Nov 29; 38(3):201-6. PubMed ID: 24601842
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  • 13. Association of Hb A2 Variants with Several Forms of α- and β-Thalassemia in Thailand.
    Panyasai S, Pornprasert S.
    Hemoglobin; 2020 May 29; 44(3):179-183. PubMed ID: 32482156
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  • 15. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM, El-Khatib FF, Ayesh S.
    Hemoglobin; 2005 May 29; 29(2):119-32. PubMed ID: 15921164
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  • 16. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
    Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK.
    Eur J Haematol; 2007 Nov 29; 79(5):417-21. PubMed ID: 17900295
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  • 19. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J, Papassotiriou I, Metaxotou-Mavrommati A, Vrettou C, Stamoulakatou A, Kanavakis E.
    Blood Cells Mol Dis; 2000 Aug 29; 26(4):276-84. PubMed ID: 11042028
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