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Journal Abstract Search

164 related items for PubMed ID: 2329681

  • 1. [A Japanese family with hereditary HbH disease--a case report and its gene analysis].
    Hattori Y, Yamashiro Y, Yamamoto K, Morishita M, Miyaji T, Yamamoto K, Matsuno Y, Fujii H, Miwa S, Ichimaru M.
    Rinsho Ketsueki; 1990 Feb; 31(2):183-8. PubMed ID: 2329681
    [Abstract] [Full Text] [Related]

  • 2. Identification of a nondeletion defect in alpha-thalassemia.
    Kan YW, Dozy AM, Trecartin R, Todd D.
    N Engl J Med; 1977 Nov 17; 297(20):1081-4. PubMed ID: 909565
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  • 3. [Double heterozygote hemoglobin D/B0 thalassemia. Report of 3 cases in a Portuguese family].
    Sousa Uva L, Fernandes A, Pilar M.
    Nouv Rev Fr Hematol (1978); 1983 Nov 17; 25(6):387-90. PubMed ID: 6664837
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  • 4. A severe alpha thalassemia case compound heterozygous for Hb Adana in alpha1 gene and 20.5 kb double gene deletion.
    Durmaz AA, Akin H, Ekmekci AY, Onay H, Durmaz B, Cogulu O, Aydinok Y, Ozkinay F.
    J Pediatr Hematol Oncol; 2009 Aug 17; 31(8):592-4. PubMed ID: 19636270
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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 17; 78(2):137-9. PubMed ID: 2828223
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  • 6. 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 Feb 17; 26 Suppl 1():252-6. PubMed ID: 8629117
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  • 7. A study on the biochemical genetics of abnormal hemoglobins.
    I-Tao T.
    Sci Sin; 1975 Feb 17; 18(4):527-44. PubMed ID: 1202635
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  • 11. 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 17; 54(6):1439-45. PubMed ID: 508947
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  • 16. 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 17; 55(3):511-6. PubMed ID: 7357081
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  • 17. [A case of a Japanese family with Hb San Diego [beta 109(G11)Val----Met]-beta zero thalassemia].
    Harano T, Ikeda N, Nibu K.
    Nihon Ketsueki Gakkai Zasshi; 1987 Nov 17; 50(7):1272-9. PubMed ID: 3445738
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  • 18. The first compound heterozygosity for HKalpha alpha allele and Southeast Asian deletion allele.
    Li Z, Cai S, Rong K, Song G, Li Y, Guo R.
    Clin Biochem; 2007 Mar 17; 40(5-6):407-10. PubMed ID: 17306786
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  • 19. Molecular characterization of HbH disease in the Cuban population.
    Martinez G, Ferreira R, Hernandez A, Di Rienzo A, Felicetti L, Colombo B.
    Hum Genet; 1986 Apr 17; 72(4):318-9. PubMed ID: 3009300
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