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Journal Abstract Search

227 related items for PubMed ID: 6449401

  • 1. [Study of the molecular causes of thalassemia. II. Deletion of alpha-globin genes in hemoglobinopathy H].
    Shipitsyna GI, Lunts MG, Shifter KA, Idel'son LI, Limborskaia SA.
    Genetika; 1980; 16(1):78-85. PubMed ID: 6449401
    [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
    [Abstract] [Full Text] [Related]

  • 3. 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 Nov 17; 26 Suppl 1():252-6. PubMed ID: 8629117
    [Abstract] [Full Text] [Related]

  • 4. [Molecular causes of thalassemia. III. Molecular genetic variants of beta-thalassemia in Azerbaijan].
    Dergunova LV, Slominskiĭ PA, Rustamov RSh, Dadasheva TS, Amzashvili MG.
    Genetika; 1982 Jul 17; 18(7):1045-55. PubMed ID: 6180957
    [Abstract] [Full Text] [Related]

  • 5. Partial deletion of the alpha-globin structural gene in human alpha-thalassaemia.
    Orkin SH, Michelson A.
    Nature; 1980 Jul 31; 286(5772):538-40. PubMed ID: 7402334
    [No Abstract] [Full Text] [Related]

  • 6. [Molecular causes of thalassemia. I. Identification of globin mRNA in homozygous beta-thalassemia using complementary human globin DNA].
    Limborskaia SA, Frolova LIu, Maleeva NE, Shipitsyna GI, Skobeleva NA.
    Mol Biol (Mosk); 1978 Jul 31; 12(4):787-94. PubMed ID: 683189
    [No Abstract] [Full Text] [Related]

  • 7. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J, Papassotiriou I, Metaxotou-Mavrommati A, Vrettou C, Stamoulakatou A, Kanavakis E.
    Blood Cells Mol Dis; 2000 Aug 31; 26(4):276-84. PubMed ID: 11042028
    [Abstract] [Full Text] [Related]

  • 8. 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 31; 67(2):469-73. PubMed ID: 3942832
    [Abstract] [Full Text] [Related]

  • 9. alpha-globin gene deletions associated with Hb J Tongariki.
    Bowden DK, Pressley L, Higgs DR, Clegg JB, Weatherall DJ.
    Br J Haematol; 1982 Jun 31; 51(2):243-9. PubMed ID: 6979350
    [Abstract] [Full Text] [Related]

  • 10. 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 31; 54(6):1434-8. PubMed ID: 508946
    [Abstract] [Full Text] [Related]

  • 11. [Analysis of a program for atypical familial microcytosis. Molecular basis of alpha-thalassemia].
    Villegas Martínez A.
    Sangre (Barc); 1990 Aug 31; 35(4):277-88. PubMed ID: 2274839
    [Abstract] [Full Text] [Related]

  • 12. Silent thalassemias: genotypes and phenotypes.
    Bianco I, Cappabianca MP, Foglietta E, Lerone M, Deidda G, Morlupi L, Grisanti P, Ponzini D, Rinaldi S, Graziani B.
    Haematologica; 1997 Aug 31; 82(3):269-80. PubMed ID: 9234571
    [Abstract] [Full Text] [Related]

  • 13. 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 31; 18(3):289-96. PubMed ID: 2983536
    [Abstract] [Full Text] [Related]

  • 14. Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.
    Bowden DK, Hill AV, Higgs DR, Oppenheimer SJ, Weatherall DJ, Clegg JB.
    J Clin Invest; 1987 Jan 31; 79(1):39-43. PubMed ID: 3793931
    [Abstract] [Full Text] [Related]

  • 15. [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; 31(2):183-8. PubMed ID: 2329681
    [Abstract] [Full Text] [Related]

  • 16. Heterogeneity of beta-thalassemia in Azerbaidzhan.
    Dergunova LV, Ryskov AP, Slominsky PA, Rustamov RS, Limborska SA.
    Haematologia (Budap); 1984 Feb 31; 17(4):473-81. PubMed ID: 6241915
    [Abstract] [Full Text] [Related]

  • 17. Thalassemic hemoglobinopathies.
    Steinberg MH, Adams JG.
    Am J Pathol; 1983 Dec 31; 113(3):396-409. PubMed ID: 6359893
    [Abstract] [Full Text] [Related]

  • 18. [Moleculo-genetic study of beta-thalassemia heterogenity in the USSR].
    Dergunova LV, Mazurova OL, Slominskiĭ PA, Limborskaia SA.
    Vopr Med Khim; 1983 Dec 31; 29(3):33-8. PubMed ID: 6308904
    [Abstract] [Full Text] [Related]

  • 19. 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 31; 146(6):264-9. PubMed ID: 6155503
    [Abstract] [Full Text] [Related]

  • 20. Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion.
    Harteveld CL, Versteegh FG, van Leer EH, Starreveld JS, Kok PJ, van Rooijen-Nijdam I, van Delft P, Zanella-Cleon I, Becchi M, Wajcman H, Giordano PC.
    Hemoglobin; 2007 Jun 31; 31(3):313-23. PubMed ID: 17654068
    [Abstract] [Full Text] [Related]

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