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PUBMED FOR HANDHELDS

Journal Abstract Search


126 related items for PubMed ID: 6814490

  • 41. Oxygen affinity and stability of hemoglobin Dunn alpha 6(A4)Asp replaced by Asn): use of isoelectric focusing in recognition of a new abnormal hemoglobin.
    Charache S, Brimhall B, Zaatari G.
    Am J Hematol; 1980; 9(2):151-60. PubMed ID: 7435503
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  • 45. [Clinical and biological studies of an hybrid S/Stanleyville II hemoglobin (alpha 2 78 Asn replaced by Lys beta 2 6 Glu replaced by Val) (author's transl)].
    North ML, Hassan W, Thillet J, Schwartz M, Taubert C, Ritter J, Gandar R, Rosa J.
    Nouv Rev Fr Hematol (1978); 1980; 22(3):235-41. PubMed ID: 6782549
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  • 47. Haemoglobin GPhiladelphia and its interaction with haemoglobin S and alpha-thalassaemia in Nigerians.
    Knox-Macaulay HH, Fleming AF, Lamb J, Mba EC.
    Clin Lab Haematol; 1984; 6(2):113-21. PubMed ID: 6488738
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  • 48. Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia.
    Honig GR, Shamsuddin M, Vida LN, Mompoint M, Valcourt E, Bowie LJ, Jones EC, Powers PA, Spritz RA, Guis M.
    J Clin Invest; 1984 Jun; 73(6):1740-9. PubMed ID: 6725558
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  • 49. Hb S, Hb G-Philadelphia and alpha-thalassemia-2 in a Black family.
    Felice AE, Mayson SM, Webber BB, Miller A, Gravely ME, Huisman TH.
    Pediatr Res; 1980 Mar; 14(3):266-7. PubMed ID: 7383748
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  • 50. Identification of Hb Lepore-Washington-Boston in association with Hb E [beta 26(B8)Glu----Lys] in a Thai female.
    Boontrakoonpoontawee P, Svasti J, Fucharoen S, Winichagoon P.
    Hemoglobin; 1987 Mar; 11(4):309-16. PubMed ID: 3667318
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  • 51. Hb F-Marietta or G gamma I 80[EF4] Asp replaced by Asn, observed in a Caucasian baby.
    Nakatsuji T, Lam H, Carver J, Huisman TH.
    Hemoglobin; 1982 Mar; 6(4):407-11. PubMed ID: 6183237
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  • 52. α-Thalassemia associated with hb instability: a tale of two features. the case of Hb Rogliano or α1 Cod 108(G15)Thr→Asn and Hb Policoro or α2 Cod 124(H7)Ser→Pro.
    Bisconte MG, Caldora M, Musollino G, Cardiero G, Flagiello A, La Porta G, Lagona L, Prezioso R, Qualtieri G, Gaudiano C, Medulla E, Merlino A, Pucci P, Lacerra G.
    PLoS One; 2015 Mar; 10(3):e0115738. PubMed ID: 25730315
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  • 53. Description of two new alpha variants: Hb Canuts [alpha85(F6)Asp-->His (alpha1)] and Hb Ambroise Pare [alpha117(GH5)Phe-->Ile (alpha2)]; two new beta variants: Hb Beaujolais [beta84(EF8)Thr-->Asn] and Hb Monplaisir [beta147 (Tyr-Lys-Leu-Ala-Phe-Phe-Leu-Leu-Ser-Asn-Phe-Tyr-158-COOH)] and one new delta variant: Hb (A2)North Africa [delta59(E3)Lys-->Met].
    Joly P, Lacan P, Bererd M, Garcia C, Zanella-Cleon I, Becchi M, Aubry M, Couprie N, Francina A.
    Hemoglobin; 2009 Mar; 33(3):196-205. PubMed ID: 19657833
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  • 54. Hb Kurdistan [alpha 47(CE5)Asp-->Tyr], a new alpha chain variant in combination with beta (0)-thalassemia.
    Giordano PC, Harteveld CL, Streng H, Oosterwijk JC, Heister JG, Amons R, Bernini LF.
    Hemoglobin; 1994 Jan; 18(1):11-8. PubMed ID: 8195005
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  • 55. Alternate organization of alpha G-Philadelphia globin genes among U.S. black and Italian Caucasian heterozygotes.
    Sciarratta GV, Sansone G, Ivaldi G, Felice AE, Huisman TH.
    Hemoglobin; 1984 Jan; 8(6):537-47. PubMed ID: 6526651
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  • 56. Hb Davenport or alpha 2(78)(EF7)Asn----His beta 2.
    Wilson JB, Webber BB, Plaseska D, de Alarcon PA, McMillan SK, Huisman TH.
    Hemoglobin; 1990 Jan; 14(6):599-605. PubMed ID: 2101836
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  • 57. Hemoglobin Dunn: alpha 6 (A4) aspartic acid replaced by asparagine.
    Jue DL, Johnson MH, Patchen LC, Moo-Penn WF.
    Hemoglobin; 1979 Jan; 3(2-3):137-43. PubMed ID: 478975
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