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 *

123 related articles for article (PubMed ID: 5694805)

  • 1. Haemoglobin H disease study of an Eti-Turk family.
    Aksoy M; Erdem S
    Acta Genet Stat Med; 1968; 18(1):12-22. PubMed ID: 5694805
    [No Abstract]   [Full Text] [Related]  

  • 2. Is haemoglobin G Philadelphia linked to -thalassaemia?
    French EA; Lehmann H
    Acta Haematol; 1971; 46(3):149-56. PubMed ID: 5001519
    [No Abstract]   [Full Text] [Related]  

  • 3. Thalassemia types among Kurdish Jews.
    Cohen T
    Isr J Med Sci; 1973; 9(9):1461-3. PubMed ID: 4359642
    [No Abstract]   [Full Text] [Related]  

  • 4. A new sickling disorder resulting from interaction of the genes for haemoglobin S and alpha-thalassaemia.
    Weatherall DJ; Clegg JB; Blankson J; McNeil JR
    Br J Haematol; 1969 Dec; 17(6):517-26. PubMed ID: 5357741
    [No Abstract]   [Full Text] [Related]  

  • 5. Haemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain.
    Milner PF; Clegg JB; Weatherall DJ
    Lancet; 1971 Apr; 1(7702):729-32. PubMed ID: 4101431
    [No Abstract]   [Full Text] [Related]  

  • 6. Haemoglobin H disease and beta-thalassaemia. Clinical haematological and electrophoretic studies in a family from South Lebanon.
    Shahid MJ; Khouri FP; Sahli IF
    J Med Genet; 1974 Sep; 11(3):275-9. PubMed ID: 4372355
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Haemoglobin Köln in a Jewish family.
    Hällén J; Charlesworth D; Lehmann H
    Acta Med Scand; 1972 Mar; 191(3):177-80. PubMed ID: 5033708
    [No Abstract]   [Full Text] [Related]  

  • 8. A case of haemoglobin J Sardegna- -thalassaemia double heterozygosis.
    Gallo E; Pugliatti L; Ricco G; Pich PG; Pinna G; Mazza U
    Acta Haematol; 1972; 47(5):311-20. PubMed ID: 4625462
    [No Abstract]   [Full Text] [Related]  

  • 9. [A2' (B2) hemoglobin associated with beta thalassemia and hereditary persistence of fetal hemoglobin. Study in 3 Colombian families].
    Echavarria A; Molina C; Zapata CI
    Sangre (Barc); 1973; 18(2):145-56. PubMed ID: 4753554
    [No Abstract]   [Full Text] [Related]  

  • 10. The incidence of -thalassemia and abnormal hemoglobins in Turkey.
    Cavdar AO; Arcasoy A
    Acta Haematol; 1971; 45(5):312-8. PubMed ID: 5000043
    [No Abstract]   [Full Text] [Related]  

  • 11. Family studies of alpha-thalassemia and hemoglobin H disease in Eastern Saudi Arabia.
    Mcniel JR
    J Med Assoc Thai; 1971 Mar; 54(3):153-66. PubMed ID: 4101839
    [No Abstract]   [Full Text] [Related]  

  • 12. Absence of haemoglobin A in an individual simultaneously heterozygous in the genes for hereditary persistence of foetal haemoglobin and beta-thalassemia.
    Fogarty WM; Vedvick TS; Itano HA
    Br J Haematol; 1974 Apr; 26(4):527-33. PubMed ID: 4846265
    [No Abstract]   [Full Text] [Related]  

  • 13. Study on nine families with haemoglobin Lepore in Campania: Hb Lepore trait, heterozygosity for Hb Lepore and beta-thalassaemia, homozygosity for Hb Lepore.
    Quattrin N; Bianchi P; Cimino R; De Rosa L; Dini E; Ventruto V
    Acta Haematol; 1967; 37(5):266-75. PubMed ID: 4963514
    [No Abstract]   [Full Text] [Related]  

  • 14. Sickle-cell anaemia, sickle-cell thalassaemia, sickle-cell haemoglobin C disease, and asymptomatic haemoglobin C thalassaemia in one Ghanaian family.
    Konotey-Ahulu FI; Ringelhann B
    Br Med J; 1969 Mar; 1(5644):607-12. PubMed ID: 5766126
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Haemoglobin anomalies in Khartoum.
    Ibrahim SA
    J Trop Med Hyg; 1970 Aug; 73(8):205-7. PubMed ID: 5492299
    [No Abstract]   [Full Text] [Related]  

  • 16. Haemoglobinopathies in Burma. II. Haemoglobin H disease.
    Aung-Than-Batu ; U-Hla-Pe ; Khin-Kyi-Nyunt
    Trop Geogr Med; 1971 Mar; 23(1):19-23. PubMed ID: 4252406
    [No Abstract]   [Full Text] [Related]  

  • 17. Haemoglobin LeporeBoston in a Turkish family.
    Cavdar AO; Arcasoy A
    J Med Genet; 1976 Oct; 13(5):363-5. PubMed ID: 1003447
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Unusual combination of genetic defects in a Sicilian family: beta-thalassaemia, haemoglobin Lepore Boston-Washington and heterocellular hereditary persistence of fetal haemoglobin.
    Schilirò G; Musumeci S; Romeo MA; Di Gregorio F; Russo A; Testa R; Russo G
    Br J Haematol; 1983 Nov; 55(3):473-7. PubMed ID: 6196048
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Association of alpha thalassemia and Hb G Philadelphia in a Spanish family].
    González Redondo JM; De Pablos JM
    Sangre (Barc); 1988 Jun; 33(3):224-8. PubMed ID: 3175819
    [No Abstract]   [Full Text] [Related]  

  • 20. Hemoglobin-A2-Coburg or alpha2delta2116Arg leads to His (G18).
    Sharma RS; Williams L; Wilson JB; Huisman TH
    Biochim Biophys Acta; 1975 Jun; 393(2):379-82. PubMed ID: 1148221
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.