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 *

174 related articles for article (PubMed ID: 4503918)

  • 1. Clinical studies and physiological properties of Hopkins-2 haemoglobin.
    Charache S; Ostertag W; von Ehrenstein G
    Nat New Biol; 1972 May; 237(72):88-90. PubMed ID: 4503918
    [No Abstract]   [Full Text] [Related]  

  • 2. Hemoglobin S-Ga Georgia disease: a case report.
    Wrightstone RN; Hubbard M; Huisman TH
    Acta Haematol; 1974; 51(5):315-20. PubMed ID: 4209499
    [No Abstract]   [Full Text] [Related]  

  • 3. Hereditary persistence of foetal haemoglobin associated with a gamma beta fusion variant, haemoglobin Kenya.
    Clegg JB; Weatherall DJ; Gilles HM
    Nat New Biol; 1973 Dec; 246(154):184-6. PubMed ID: 4519001
    [No Abstract]   [Full Text] [Related]  

  • 4. [Interactions between Stanleyville 2 and S hemoglobins in a family from Zaire. Study of the Stanleyville 2-S hybrid (alpha 2-78Lys beta 2-6 Val)].
    Van Ros G; Wiltshire B; Renoirte-Monjoie AM; Vervoort T; Lehmann H
    Biochimie; 1973; 55(9):1107-19. PubMed ID: 4785223
    [No Abstract]   [Full Text] [Related]  

  • 5. Duplicated alpha-chain genes in Hopkins-2 haemoglobin of man and evidence for unequal crossing over between them.
    Ostertag W; von Ehrenstein G; Charache S
    Nat New Biol; 1972 May; 237(72):90-4. PubMed ID: 4503919
    [No Abstract]   [Full Text] [Related]  

  • 6. Hemoglobin O arab in four negro families and its interaction with hemoglobin S and hemoglobin C.
    Milner PF; Miller C; Grey R; Seakins M; DeJong WW; Went LN
    N Engl J Med; 1970 Dec; 283(26):1417-25. PubMed ID: 5481775
    [No Abstract]   [Full Text] [Related]  

  • 7. Hemoglobin G-Philadelphia-S. A family study of an inherited hybrid hemoglobin.
    Rising JA; Sautter RL; Spicer SJ
    Am J Clin Pathol; 1974 Jan; 61(1):92-102. PubMed ID: 4809151
    [No Abstract]   [Full Text] [Related]  

  • 8. Hemoglobin Tochigi disease, a new unstable hemoglobin hemolytic anemia found in a Japanese family.
    Yamada K; Shinkai N; Nakazawa S; Yamada Z; Saito K
    Nihon Ketsueki Gakkai Zasshi; 1971 Aug; 34(4):484-97. PubMed ID: 5170457
    [No Abstract]   [Full Text] [Related]  

  • 9. Haemoglobin Bart's and slow-moving haemoglobin x components in newborns. The homozygous state for the slow-moving X components in a Malay boy.
    Lie-Injo LE
    Acta Haematol; 1973; 49(1):25-35. PubMed ID: 4632449
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Double heterozygosity for hemoglobin G (alpha-2 68Lys beta-A2) and hemoglobin D (alpha A2-beta-121Gln).
    Rothman MC; Ranney HM
    Blood; 1971 Feb; 37(2):177-83. PubMed ID: 5549195
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Multiple alpha chain loci for human haemoglobins: Hb J-Buda and Hb G-Pest.
    Hollán SR; Szelenyi JG; Brimhall G; Duerst M; Jones RT; Koler RD; Stocklen Z
    Nature; 1972 Jan; 235(5332):47-50. PubMed ID: 4550395
    [No Abstract]   [Full Text] [Related]  

  • 14. 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
    [No Abstract]   [Full Text] [Related]  

  • 15. The molecular basis of hemoglobin disease.
    Stamatoyannopoulos G
    Annu Rev Genet; 1972; 6():47-70. PubMed ID: 4581487
    [No Abstract]   [Full Text] [Related]  

  • 16. Haemoglobin Ocho Rios ( beta52 (D3) aspartic acid leads to alanine): a new beta-chain variant of haemoglobin A found in combination with haemoglobin S.
    Beresford CH; Clegg JB; Weatherall DJ
    J Med Genet; 1972 Jun; 9(2):151-3. PubMed ID: 5046622
    [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. 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]  

  • 19. 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]  

  • 20. Inheritance of haemoglobin H disease. A new aspect.
    Lie-Injo LE; Lopez CG; Lopes M
    Acta Haematol; 1971; 46(2):106-20. PubMed ID: 4331171
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.