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Journal Abstract Search

133 related items for PubMed ID: 508947

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  • 3. A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait.
    Steinberg MH, Coleman MB, Adams JG, Hartmann RC, Saba H, Anagnou NP.
    Blood; 1986 Feb; 67(2):469-73. PubMed ID: 3942832
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  • 5. Mapping the alpha-globin genes in an Algerian HbH patient and his family.
    Whitelaw E, Pagnier J, Verdier G, Henni T, Godet J, Williamson R.
    Blood; 1980 Mar; 55(3):511-6. PubMed ID: 7357081
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  • 6. The varied arrangement of the alpha globin genes in alpha thalassemia and Hb H disease in American blacks.
    Sancar GB, Cedeno MM, Rieder RF.
    Johns Hopkins Med J; 1980 Jun; 146(6):264-9. PubMed ID: 6155503
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  • 9. Linkage of alpha G-Philadelphia to alpha-thalassemia in African-Americans .
    Surrey S, Ohene-Frempong K, Rappaport E, Atwater J, Schwartz E.
    Proc Natl Acad Sci U S A; 1980 Aug; 77(8):4885-9. PubMed ID: 6933536
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  • 10. The molecular basis of HbH disease in Taiwan.
    Peng HW, Han SH, Chow TY, Ho CH, Ching KN, Chiang BN.
    Hum Genet; 1988 Feb; 78(2):137-9. PubMed ID: 2828223
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  • 11. Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.
    Lie-Injo LE, Herrera AR, Lebo RV, Hassan K, Lopez CG.
    Am J Hematol; 1985 Mar; 18(3):289-96. PubMed ID: 2983536
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  • 13. Alpha-globin gene deletion causes alpha-thalassemia syndromes in two German families.
    Horst J, Griese EU, Kleihauer E, Kohne E.
    Hum Genet; 1984 Mar; 68(3):260-3. PubMed ID: 6094337
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  • 14. Partial deletion of the alpha-globin structural gene in human alpha-thalassaemia.
    Orkin SH, Michelson A.
    Nature; 1980 Jul 31; 286(5772):538-40. PubMed ID: 7402334
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  • 16. Genetic and molecular diversity in nondeletion Hb H disease.
    Higgs DR, Pressley L, Aldridge B, Clegg JB, Weatherall DJ, Cao A, Hadjiminas MG, Kattamis C, Metaxatou-Mavromati A, Rachmilewitz EA, Sophocleous T.
    Proc Natl Acad Sci U S A; 1981 Sep 31; 78(9):5833-7. PubMed ID: 6272319
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  • 19. Phenotype-genotype correlation in haemoglobin H disease in childhood.
    Galanello R, Pirastu M, Melis MA, Paglietti E, Moi P, Cao A.
    J Med Genet; 1983 Dec 31; 20(6):425-9. PubMed ID: 6317863
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