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PUBMED FOR HANDHELDS

Journal Abstract Search

287 related items for PubMed ID: 7255798

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  • 2. [Drepanocytosis and genetics].
    Laurens A, Diakhate L, Blavy G, Diebolt G, Linhard J.
    Bull Soc Med Afr Noire Lang Fr; 1978; 23(4):441-4. PubMed ID: 755529
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  • 3. A rare case of a compound heterozygote hemoglobin S/hemoglobin Fannin-Lubbock-I individual. Is it a sickling disorder?
    Burns NK, Risin SA.
    Lab Hematol; 2010 Jun; 16(2):26-7. PubMed ID: 20534428
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  • 8. [Systematic screening of hemoglobinopathies in blood donors in Guadeloupe (French West Indies)].
    Fabritius H, Millan J, Le Corroller Y.
    Rev Fr Transfus Immunohematol; 1978 Sep; 21(4):937-50. PubMed ID: 734306
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  • 11. Haemoglobin SD disease--rare case of jaundice.
    Ghosh UC, Sen K, Narayan A, Banik KK, Saha PK.
    J Indian Med Assoc; 2012 Jul; 110(7):501-2. PubMed ID: 23520682
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  • 17. The clinical importance of abnormal human hemoglobins. II.
    Cawein MJ, Lappat EJ.
    Med Times; 1967 Nov; 95(11):1156-70. PubMed ID: 6081099
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  • 18. Screening newborn infants for sickle hemoglobin.
    Pegelow CH, Pitel P, Judisch J, Randall-David E, Siderits P, Ausbon W.
    J Fla Med Assoc; 1988 Oct; 75(10):670-5. PubMed ID: 2461429
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  • 19. [Familial study of Hb A2 Babinga (delta 136 Glyc----Asp) in South America].
    Jaeger G, Malambo J, Coquelet ML, Barbet MC, Brumpt LC.
    Bull Soc Pathol Exot Filiales; 1985 Oct; 78(1):89-93. PubMed ID: 3986955
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  • 20. Spectrophotometric quantitation of haemoglobin S fraction in heterozygous sickle-cell trait (HbAS).
    Reid HL, Famodu AA.
    Med Lab Sci; 1988 Apr; 45(2):143-5. PubMed ID: 3210920
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