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Journal Abstract Search

169 related items for PubMed ID: 6437117

  • 1. Haemoglobin E variants: a clinical, haematological and biosynthetic study of 4 South African families.
    Bird AR, Wood K, Leisegang F, Mathew CG, Ellis P, Hartley PS, Karabus CD.
    Acta Haematol; 1984; 72(2):135-7. PubMed ID: 6437117
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  • 3. Globin synthesis in subjects doubly heterozygous for hemoglobin G-Philadelphia and hemoglobin S or C.
    McCurdy PR, Sherman AS, Kamuzora H, Lehmann H.
    J Lab Clin Med; 1975 Jun; 85(6):891-7. PubMed ID: 1138022
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  • 4. Molecular and haematological characterization of compound Hb E/Hb Pyrgos and Hb E/Hb J-Bangkok in Thai patients.
    Fucharoen S, Singsanan S, Sanchaisuriya K, Fucharoen G.
    Clin Lab Haematol; 2005 Jun; 27(3):184-9. PubMed ID: 15938724
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  • 7. Hemoglobin sickle-Lepore: report of two siblings and review of the literature.
    Seward DP, Ware RE, Kinney TR.
    Am J Hematol; 1993 Nov; 44(3):192-5. PubMed ID: 8213769
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  • 8. Haemoglobin Lepore Boston-Washington in Sicily: clinical, haematological, and biosynthetic studies.
    Schiliro G, Musumeci S, Pizzarelli G, Fischer A, Romero MA, Russo G.
    J Med Genet; 1980 Jun; 17(3):179-82. PubMed ID: 7401128
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  • 10. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy.
    Sanchaisuriya K, Chunpanich S, Fucharoen S, Fucharoen G, Sanchaisuriya P, Changtrakun Y.
    Eur J Haematol; 2005 Mar; 74(3):221-7. PubMed ID: 15693792
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  • 11. [Erythrocyte hypocromia in heterozygous hemoglobin E (beta 26 Glu replaced by Lys)].
    Keller P, Kohne E.
    Acta Haematol; 1976 Mar; 56(5):276-84. PubMed ID: 826084
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  • 12. 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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  • 13. Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.
    Tan J, Tay JS, Wong YC, Kham SK, Bte Abd Aziz N, Teo SH, Wong HB.
    Southeast Asian J Trop Med Public Health; 1995 Jun; 26 Suppl 1():252-6. PubMed ID: 8629117
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  • 16. Hb Sheffield [β58(E2)Pro→His] in Oman: potential pitfall in genetic counseling.
    Al Zadjali S, Daar S, AlKindi S, Gravell D, Al Haddabi H, Berbar T, Krishnamoorthy R.
    Hemoglobin; 2011 Jun; 35(2):111-6. PubMed ID: 21417567
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  • 17. Double heterozygous hemoglobinopathies--diagnostic importance of parent studies.
    Patra SB, Giri DD, Patel RZ, Modi UJ, Amin NS.
    Indian Pediatr; 1983 Jul; 20(7):485-8. PubMed ID: 6654480
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  • 19. Cord blood study on beta-thalassemia and hemoglobin E.
    Pootrakul S, Muang-sup V, Fucharoen S, Wasi P.
    Am J Med Genet; 1988 Jan; 29(1):49-57. PubMed ID: 2449818
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  • 20. [Diagnosis of thalassemias and hemoglobinopathies by HPLC (high performance liquid chromatography): study of 627 patients].
    Sabo G, Brodbeck U, Cardile N, Viollier AF, Scheurmann T, Knecht H.
    Schweiz Med Wochenschr; 1999 Aug 28; 129(34):1196-200. PubMed ID: 10486859
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