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Journal Abstract Search

132 related items for PubMed ID: 2599878

  • 1. Hb Fontainebleau [alpha 21(B2)Ala----pro], a new silent mutant hemoglobin.
    Wajcman H, Blouquit Y, Gombaud-Saintonge G, Riou J, Galacteros F.
    Hemoglobin; 1989; 13(5):421-8. PubMed ID: 2599878
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  • 2. A second case of Hb Fontainebleau [alpha21(B2)Ala-->Pro] in an individual with microcytosis.
    Brennan SO, Chan T, Ryken S, Ruskova A.
    Hemoglobin; 2009; 33(3):258-61. PubMed ID: 19657841
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  • 3. Hb Long Island: a hemoglobin variant with a methionyl extension at the NH2 terminus and a prolyl substitution for the normal histidyl residue 2 of the beta chain.
    Barwick RC, Jones RT, Head CG, Shih MF, Prchal JT, Shih DT.
    Proc Natl Acad Sci U S A; 1985 Jul; 82(14):4602-5. PubMed ID: 3860812
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  • 4. Hb Brockton [alpha 2 beta 2138(H16)Ala----Pro] observed in a Turkish girl.
    Ulukutlu L, Ozsahin H, Wilson JB, Webber BB, Hu H, Kutlar A, Kutlar F, Huisman TH.
    Hemoglobin; 1989 Jul; 13(5):509-13. PubMed ID: 2599887
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  • 8. Hemoglobin Hobart or alpha 20(Bl)His----Arg: a new alpha chain hemoglobin variant.
    Fleming PJ, Sumner DR, Wyatt K, Hughes WG, Melrose WD, Jupe DM, Baikie MJ.
    Hemoglobin; 1987 Jul; 11(3):211-20. PubMed ID: 3654264
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  • 9. Germline mosaicism for an alanine to valine substitution at residue beta 140 in hemoglobin Puttelange, a new variant with high oxygen affinity.
    Wajcman H, Girodon E, Promé D, North ML, Plassa F, Duwig I, Kister J, Bergerat JP, Oberling F, Lampert E.
    Hum Genet; 1995 Dec; 96(6):711-6. PubMed ID: 8522332
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  • 10. Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband.
    Sidhwa K, Daruwalla MR, Pawar R, Nadkarni A, Hariharan P, Mehta P, Gupta AD.
    Indian J Pathol Microbiol; 2019 Dec; 62(2):323-325. PubMed ID: 30971568
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  • 11. A new unstable and low oxygen affinity hemoglobin variant: Hb Stanmore [beta 111(G13)Val----Ala].
    Como PF, Wylie BR, Trent RJ, Bruce D, Volpato F, Wilkinson T, Kronenberg H, Holland RA, Tibben EA.
    Hemoglobin; 1991 Dec; 15(1-2):53-65. PubMed ID: 1917537
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  • 12. Hemoglobin Shuangfeng (alpha 27 (B8) Glu substituting for Lys): a new unstable hemoglobin variant.
    Chihchuan L, Hainan T, Hweiyuen L, Shangzhi H, Ruiyou L, Bauseng W.
    Hemoglobin; 1981 Dec; 5(7-8):691-700. PubMed ID: 7338471
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  • 13. Hemoglobin Brockton [beta 138 (H16) Ala----Pro]: an unstable variant near the C-terminus of the beta-subunits with normal oxygen-binding properties.
    Moo-Penn WF, Jue DL, Johnson MH, Olsen KW, Shih D, Jones RT, Lux SE, Rodgers P, Arnone A.
    Biochemistry; 1988 Oct 04; 27(20):7614-9. PubMed ID: 3207692
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  • 17. Hemoglobin Evanston: alpha 14(A12) Trp leads to Arg. A variant hemoglobin associated with alpha-thalassemia-2.
    Moo-Penn WF, Baine RM, Jue DL, Johnson MH, McGuffey JE, Benson JM.
    Biochim Biophys Acta; 1983 Sep 14; 747(1-2):65-70. PubMed ID: 6882779
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  • 18. Characterization of a new electrophoretically silent hemoglobin variant. Hb saale OR alpha 2beta 2 84(EF8)Thr --> Ala.
    Bissé E, Zorn N, Heinrichs I, Eigel A, Van Dorsselaer A, Wieland H, Kister J, Marden MC.
    J Biol Chem; 2000 Jul 14; 275(28):21380-4. PubMed ID: 10770934
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  • 19. Hb Val de Marne [alpha 133(H16)Ser-->Arg]: a new hemoglobin variant with moderate increase in oxygen affinity.
    Wajcman H, Kister J, M'Rad A, Marden MC, Riou J, Galacteros F.
    Hemoglobin; 1993 Oct 14; 17(5):407-17. PubMed ID: 8294200
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  • 20. Hb Iraq-Halabja beta10 (A7) Ala-->Val (GCC-->GTC): a new beta-chain silent variant in a family with multiple Hb disorders.
    Deutsch S, Darbellay R, Offord R, Frutiger A, Kister J, Wajcman H, Beris P.
    Am J Hematol; 1999 Jul 14; 61(3):187-93. PubMed ID: 10398311
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