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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

560 related items for PubMed ID: 16798637

  • 21.
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  • 22. Hb Nile[A1] and Hb Nile[A2]: novel identical [alpha77(EF6)Pro-->Ser] variants found in either the alpha1- or alpha2-globin genes.
    van Zwieten R, Kaufmann JO, Vuil H, Kouwenberg J, Verhoeven AJ, Fogelberg K, Harteveld CL, Giordano PC.
    Hemoglobin; 2009; 33(3):188-95. PubMed ID: 19657832
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  • 23. Hb La Coruña [beta38(C4)Thr-->Ile]: a new hemoglobin variant leading to familial polycythemia.
    Ropero P, Fernández-Lago C, Villegas A, Polo M, Mateo M, Mora A, González FA.
    Hemoglobin; 2006; 30(3):379-83. PubMed ID: 16840229
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  • 25. A new alpha-globin variant with increased oxygen affinity in a Swiss family: Hb Frauenfeld [alpha 138(H21)Ser-->Phe, TCC>TTC (alpha 2)].
    Hochuli M, Zurbriggen K, Schmid M, Speer O, Rochat P, Frauchiger B, Kleinert P, Schmugge M, Troxler H.
    Hemoglobin; 2009; 33(1):54-8. PubMed ID: 19205974
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  • 27. Hb Charlieu [alpha106(G13)Leu-->Pro (alpha1)]: a new phenotypically silent hemoglobin variant associated with a mild alpha-thalassemia phenotype.
    Joly P, Szymanowicz A, Neyron MJ, Zine A, Wajcman H, Francina A.
    Hemoglobin; 2010; 34(4):366-73. PubMed ID: 20642334
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  • 28. Hb Bronte or alpha93(FG5)Val-->Gly: a new unstable variant of the alpha2-globin gene, associated with a mild alpha(+)-thalassemia phenotype.
    Lacerra G, Testa R, De Angioletti M, Schilirò G, Carestia C.
    Hemoglobin; 2003 Aug; 27(3):149-59. PubMed ID: 12908799
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  • 29. Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation.
    Moumni I, Zorai A, Daoued BB, Mosbahi I, Omar S, Kaabachi N, Dellagi K, Abbes S.
    Hemoglobin; 2007 Aug; 31(1):23-9. PubMed ID: 17365002
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  • 34. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.
    Viprakasit V, Tanphaichitr VS, Veerakul G, Chinchang W, Petrarat S, Pung-Amritt P, Higgs DR.
    Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697
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  • 38. 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; 61(3):187-93. PubMed ID: 10398311
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