BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 4753554)

  • 1. [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]  

  • 2. 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]  

  • 3. Hemoglobinopathies in a hospital population in Vancouver.
    Gray GR; Marion RB
    Can Med Assoc J; 1978 Oct; 119(7):701-4. PubMed ID: 709469
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Regulation of the beta- and delta-hemoglobin genes. A family with hereditary persistent fetal hemoglobin and beta-thalassemia.
    Rothschild H; Bickers J; Marcus R
    Acta Haematol; 1976; 56(5):285-91. PubMed ID: 826085
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Double heterozygote for beta-delta thalassaemia and S haemoglobin (author's transl)].
    de Contardi NW; Barros CA
    Sangre (Barc); 1975; 20(1):56-62. PubMed ID: 1124469
    [No Abstract]   [Full Text] [Related]  

  • 6. Hemoglobin constant spring (HbCS) and CS type hemoglobin H disease: a 3 family survey.
    Qin W; Chen Q; Yue X; Li C; Chen G; Du S
    Chin Med J (Engl); 1979 Nov; 92(11):787-92. PubMed ID: 116823
    [No Abstract]   [Full Text] [Related]  

  • 7. [Laboratory investigation of hemoglobinopathies (author's transl)].
    Naoum PC
    Rev Bras Pesqui Med Biol; 1979 Jun; 12(2-3):213-21. PubMed ID: 42121
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The interaction of alpha-thalassaemia and haemoglobin G Philadelphia.
    Rieder RF; Woodbury DH; Rucknagel DL
    Br J Haematol; 1976 Feb; 32(2):159-65. PubMed ID: 1247489
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Concurrence on two siblings of three haemoglobin abnormal genes: haemoglobin S, beta-thalassaemia and hereditary persistence of foetal haemoglobin (author's transl)].
    Guerrero García R; Rosillo de León J; Landero de Ruíz N; Padilla C; Ruíz Reyes G
    Sangre (Barc); 1978; 23(5):578-86. PubMed ID: 741340
    [No Abstract]   [Full Text] [Related]  

  • 10. The hereditary persistence of fetal hemoglobin syndromes: variations on the thalassemia theme.
    Kazazian HH
    Johns Hopkins Med J; 1976 Nov; 139(5):215-9. PubMed ID: 994361
    [No Abstract]   [Full Text] [Related]  

  • 11. Further studies of the frequency and significance of the Tgamma-chain of human fetal hemoglobin.
    Schroeder WA; Huisman TH; Efremov GD; Shelton JR; Shelton JB; Phillips R; Reese A; Gravely M; Harrison JM; Lam H
    J Clin Invest; 1979 Feb; 63(2):268-75. PubMed ID: 429552
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Observations on the rate and mechanism of hemolysis in individuals with Hb Zürich [His E7 (63)beta leads to Arg]: I. Concentrations of haptoglobin and hemopexin in the serum.
    Zinkham WH; Vangrov JS; Dixon SM; Hutchison JL
    Johns Hopkins Med J; 1979 Feb; 144(2):37-40. PubMed ID: 762915
    [No Abstract]   [Full Text] [Related]  

  • 13. Prevalence of hemoglobinopathies in north Jordan.
    Bashir N; Barkawi M; Sharif L; Momani A; Gharaibeh N
    Trop Geogr Med; 1992 Jan; 44(1-2):122-5. PubMed ID: 1379763
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haemoglobinopathy survey in an Eti-Turk village.
    Ozsoylu S; Sahinoglu M
    Hum Hered; 1975; 25(1):50-9. PubMed ID: 1150294
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Not the beta-thalassemia syndrome but hemoglobinopathy H. Studies of 3 clinical cases].
    Leo GC; Rivasi P; De Palma M; Secchi-Trinelli E; Milanti G; Silingardi R
    Minerva Med; 1977 Apr; 68(19):1293-300. PubMed ID: 854229
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in one of the regions of Azerbaijan: mass screening and laboratory investigations.
    Javadov RB; Grinberg LN; Krasnova SN; Makhmudova SA; Troitskaya OV
    Acta Biol Med Ger; 1977; 36(5-6):709-15. PubMed ID: 146387
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Interaction of Hb A2 Indonesia trait with beta-thalassaemia trait and with Hb E trait.
    Ganesan J; Lie-Injo LE
    Acta Haematol; 1978; 59(6):341-7. PubMed ID: 97892
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Kenya form of hereditary persistence of fetal haemoglobin: structural studies and evidence for homogeneous distribution of haemoglobin F using fluorescent anti-haemoglobin F antibodies.
    Nute PE; Wood WG; Stamatoyannopoulos G; Olweny C; Failkow PJ
    Br J Haematol; 1976 Jan; 32(1):55-63. PubMed ID: 1259926
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Swiss family with hemoglobin P Galveston beta117His leads to Arg, including two patients with hb P/beta thalassemia.
    Di Iorio EE; Winterhalter KH; Wilson K; Rosenmund A; Marti HR
    Blut; 1975 Aug; 31(2):61-8. PubMed ID: 1164567
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Blood-donor homozygous for hereditary persistence of fetal haemoglobin.
    Acquaye CT; Oldham JH; Konotey-Ahulu FI
    Lancet; 1977 Apr; 1(8015):796-7. PubMed ID: 66588
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.