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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

119 related items for PubMed ID: 427029

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  • 25. Beta-thalassemia in the American Negro.
    Friedman S, Hamilton RW, Schwartz E.
    J Clin Invest; 1973 Jun; 52(6):1453-9. PubMed ID: 4703230
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  • 30. -thalassemia in the American Negro.
    Schwartz E, Atwater J.
    J Clin Invest; 1972 Feb; 51(2):412-8. PubMed ID: 5061833
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  • 32. 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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  • 34. 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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  • 36. Atypical HbH disease in a Surinamese patient resulting from a combination of the -SEA and -alpha 3.7 deletions with HbC heterozygosity.
    Giordano PC, Harteveld CL, Michiels JJ, Terpstra W, Batelaan D, van Delft P, Plug RJ, van der Wielen MJ, Losekoot M, Bernini LF.
    Br J Haematol; 1997 Mar; 96(4):801-5. PubMed ID: 9074424
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  • 37. Clinical severity of non-deletion form of HbH disease (--Med/alpha alpha thal).
    Di Marzo R, Lo Gioco P, Giambona A, Acuto S, Sammarco P, Oddo G, Maggio A.
    Scand J Haematol; 1986 Jan; 36(1):39-43. PubMed ID: 3006223
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