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Journal Abstract Search

241 related items for PubMed ID: 2722997

  • 41. The levels of zeta, gamma, and delta chains in patients with Hb H disease.
    Kutlar F, Gonzalez-Redondo JM, Kutlar A, Gurgey A, Altay C, Efremov GD, Kleman K, Huisman TH.
    Hum Genet; 1989 May; 82(2):179-86. PubMed ID: 2566576
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  • 43. Bilirubin peak can be mistaken as Hb Bart's or Hb H on High-performance liquid chromatography.
    Kar R, Sharma CB.
    Hemoglobin; 2011 May; 35(2):171-4. PubMed ID: 21417577
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  • 45. Heterogeneity of fetal hemoglobin in severe alpha-thalassemia.
    Vedvick TS, Wheeler SA, Koenig HM.
    Biol Neonate; 1979 May; 36(3-4):181-4. PubMed ID: 486608
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  • 49. Is cellulose acetate electrophoresis a suitable technique for detection of Hb Bart's at birth?
    Desai S, Colah R, Gupte S, Mohanty D.
    Hum Hered; 1997 May; 47(4):181-4. PubMed ID: 9239503
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  • 55. Potential new approaches to the management of the Hb Bart's hydrops fetalis syndrome: the most severe form of α-thalassemia.
    King AJ, Higgs DR.
    Hematology Am Soc Hematol Educ Program; 2018 Nov 30; 2018(1):353-360. PubMed ID: 30504332
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  • 58. Hemoglobin alpha chain deficiency in black children with variable quantities of hemoglobin Bart's at birth.
    Altay C, Ringelhann B, Yawson GI, Bruce-Tagoe AA, Konotey-Ahulu FI, James L, Gravely M, Huisman TH.
    Pediatr Res; 1977 Feb 30; 11(2):147-52. PubMed ID: 840505
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