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Journal Abstract Search

148 related items for PubMed ID: 2878610

  • 1. Molecular basis for HbH disease in Italy: geographical distribution of deletional and nondeletional alpha-thalassemia haplotypes.
    Di Rienzo A, Novelletto A, Aliquò MC, Bianco I, Tagarelli A, Brancati C, Colombo B, Felicetti L.
    Am J Hum Genet; 1986 Nov; 39(5):631-9. PubMed ID: 2878610
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  • 2. Molecular basis of hemoglobin-H disease in the Mediterranean population.
    Kan YW, Dozy AM, Stamatoyannopoulos G, Hadjiminas MG, Zachariades Z, Furbetta M, Cao A.
    Blood; 1979 Dec; 54(6):1434-8. PubMed ID: 508946
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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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  • 4. 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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  • 5. 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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  • 6. A molecular marker associated with mild hemoglobin H disease.
    George E, Ferguson V, Yakas J, Kronenberg H, Trent RJ.
    Pathology; 1989 Jan; 21(1):27-30. PubMed ID: 2762043
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  • 7. 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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  • 8. A molecular basis for hemoglobin-H disease in American blacks.
    Phillips JA, Scott AF, Smith KD, Young KE, Lightbody KL, Jiji RM, Kazazian HH.
    Blood; 1979 Dec; 54(6):1439-45. PubMed ID: 508947
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  • 12. 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. Clinical features and molecular analysis in Thai patients with HbH disease.
    Laosombat V, Viprakasit V, Chotsampancharoen T, Wongchanchailert M, Khodchawan S, Chinchang W, Sattayasevana B.
    Ann Hematol; 2009 Dec; 88(12):1185-92. PubMed ID: 19390853
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  • 14. Beta A and beta thal DNA haplotypes in Sicily.
    Maggio A, Acuto S, Lo Gioco P, Di Marzo R, Giambona A, Sammarco P, Caronia F.
    Hum Genet; 1986 Mar; 72(3):229-30. PubMed ID: 3007327
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  • 15. Leftward deletion alpha-thalassaemia in the Saudi Arabian population.
    el-Hazmi MA.
    Hum Genet; 1986 Nov; 74(3):219-22. PubMed ID: 2430881
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  • 16. 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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  • 17. An alpha-globin gene initiation codon mutation in a black family with HbH disease.
    Olivieri NF, Chang LS, Poon AO, Michelson AM, Orkin SH.
    Blood; 1987 Sep; 70(3):729-32. PubMed ID: 3620699
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