These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 93489)

  • 21. Interaction between homozygous beta (0) thalassaemia and the Swiss type of hereditary persistence of fetal haemoglobin.
    Cappellini MD; Fiorelli G; Bernini LF
    Br J Haematol; 1981 Aug; 48(4):561-72. PubMed ID: 6168279
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Spanish delta-beta-thalassemia: hematological studies and composition of the gamma-chains in ten homozygous patients.
    Baiget M; Gimferrer E; Fernández I; Romero C; Mira Y; Pérez ML; Miguel A
    Acta Haematol; 1983; 70(5):341-4. PubMed ID: 6194643
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The Negro variety of hereditary persistence of fetal haemoglobin is a mild form of thalassaemia.
    Charache S; Clegg JB; Weatherall DJ
    Br J Haematol; 1976 Dec; 34(4):527-34. PubMed ID: 990187
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Homozygous beta thalassaemia in Liberia.
    Willcox MC; Weatherall DJ; Clegg JB
    J Med Genet; 1975 Jun; 12(2):165-73. PubMed ID: 1142380
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Thalassaemia in the British.
    Knox-Macaulay HH; Weatherall DJ; Clegg JB; Pembrey ME
    Br Med J; 1973 Jul; 3(5872):150-5. PubMed ID: 4124395
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Homozygous beta-thalassemia in Algeria. Study of 50 cases].
    Adjrad L; Rouabhi F; Amara A; Girot R; Labie D; Benabadji M
    Presse Med; 1985 Nov; 14(41):2089-92. PubMed ID: 2934707
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Association of heterocellular HPFH, beta(+)-thalassaemia, and delta beta(0)-thalassaemia: haematological and molecular aspects.
    Cianetti L; Care A; Sposi NM; Giampaolo A; Calandrini M; Petrini M; Massa A; Marinucci M; Mavilio F; Ceccanti M
    J Med Genet; 1984 Aug; 21(4):263-7. PubMed ID: 6208362
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The Corfu delta beta thalassaemia mutation in Greece: haematological phenotype and prevalence.
    Traeger-Synodinos J; Tzetis M; Kanavakis E; Metaxotou-Mavromati A; Kattamis C
    Br J Haematol; 1991 Oct; 79(2):302-5. PubMed ID: 1720325
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Homozygous delta-beta-thalassaemia in a Spanish woman.
    Gimferrer E; Baiget M; Rutllant MI
    Acta Haematol; 1979; 61(4):226-9. PubMed ID: 108904
    [No Abstract]   [Full Text] [Related]  

  • 30. The heterogeneity of normal Hb A2-beta thalassaemia in Greece.
    Kattamis C; Metaxotou-Mavromati A; Wood WG; Nash JR; Weatherall DJ
    Br J Haematol; 1979 May; 42(1):109-23. PubMed ID: 465353
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Interaction of alpha and beta thalassaemia genes in two Sardinian families.
    Furbetta M; Galanello R; Ximenes A; Angius A; Melis MA; Serra P; Cao A
    Br J Haematol; 1979 Feb; 41(2):203-10. PubMed ID: 427030
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Globin chain synthesis in the greek type (A gamma) of hereditary persisitence of fetal haemoglobin.
    Sofroniadou K; Wood WG; Nute PE; Stamatoyannopoulos G
    Br J Haematol; 1975 Jan; 29(1):137-48. PubMed ID: 1201197
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Beta-thalassaemia-87 C-->G: relationship of the Hb F modulation and polymorphisms in compound heterozygous patients.
    De Angioletti M; Lacerra G; Pagano L; Alessi M; D'Avino R; Manca L; Carestia C
    Br J Haematol; 2004 Sep; 126(5):743-9. PubMed ID: 15327529
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Nature of foetal haemoglobin in F-thalassaemia.
    Stamatoyannopoulos G; Schroeder WA; Huisman TH; Shelton JR; Shelton JB; Apell G; Bouver N
    Br J Haematol; 1971 Dec; 21(6):633-42. PubMed ID: 5132948
    [No Abstract]   [Full Text] [Related]  

  • 35. Clinical, haematological, and genetic studies of type 2 normal Hb A2 beta thalassaemia.
    Metaxotou-Mavromati A; Kattamis C; Matathia L; Tzetis M; Kanavakis E
    J Med Genet; 1988 Mar; 25(3):195-9. PubMed ID: 3351907
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hb S(C)-beta+-thalassaemia: different mutations are associated with different levels of normal Hb A.
    Gonzalez-Redondo JM; Kutlar F; Kutlar A; Stoming TA; de Pablos JM; Kilinç Y; Huisman TH
    Br J Haematol; 1988 Sep; 70(1):85-9. PubMed ID: 2460127
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Haplotypes and levels of fetal hemoglobin and G gamma to A gamma ratios in Mediterranean patients with thalassemia minor and major.
    Aksoy M; Kutlar A; Efremov GD; Nikolov N; Petkov G; Reese AL; Harano T; Chen SS; Huisman TH
    Am J Hematol; 1985 Sep; 20(1):7-16. PubMed ID: 2411130
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Haemoglobin E-beta-thalassaemia; a study of eight cases in Northwest India.
    Ghosh K; Chakrabarty AK; Mohanty D; Das KC
    Trop Geogr Med; 1983 Sep; 35(3):267-71. PubMed ID: 6196886
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The association of sickle cell anemia with heterozygous and homozygous alpha-thalassemia-2: in vitro HB chain synthesis.
    Felice AE; Webber B; Miller A; Mayson SM; Harris HF; Henson JB; Gravely ME; Huisman TH
    Am J Hematol; 1979; 6(2):91-106. PubMed ID: 474574
    [No Abstract]   [Full Text] [Related]  

  • 40. Delta beta-thalassemia in a Mexican family: clinical differences among homozygotes.
    Reyes GR; Piña-Camara A; Felice AE; Gravely ME; Huisman TH
    Hemoglobin; 1978; 2(6):513-29. PubMed ID: 750552
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.