BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

374 related articles for article (PubMed ID: 5438669)

  • 21. A study on the biochemical genetics of abnormal hemoglobins.
    I-Tao T
    Sci Sin; 1975; 18(4):527-44. PubMed ID: 1202635
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The genetics of alpha-thalassemia in Yemenite and Iraqi Jews.
    Zaizov R; Kirschmann C; Matoth Y; Adam A
    Isr J Med Sci; 1973; 9(9):1457-60. PubMed ID: 4775132
    [No Abstract]   [Full Text] [Related]  

  • 23. [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]  

  • 24. [Hemoglobin of the African newborn infant. Results of an investigation in Senegal].
    Oudart JL; Diadhiou F; Sarrat H; Satgé P
    Ann Pediatr (Paris); 1968 Dec; 15(12):773-81. PubMed ID: 4894442
    [No Abstract]   [Full Text] [Related]  

  • 25. Hematologic data in 825 cases of beta-thalassemia trait in Spain.
    Calero F; Villegas A; Porres A; Valverde F; del Potro E; Sánchez P; Luque JM; Espinós D
    Nouv Rev Fr Hematol (1978); 1990; 32(4):265-70. PubMed ID: 1705322
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The silent carrier of beta thalassemia.
    Schwartz E
    N Engl J Med; 1969 Dec; 281(24):1327-33. PubMed ID: 5355437
    [No Abstract]   [Full Text] [Related]  

  • 27. [Heterozygous beta thalassemia with increased HbF: independent segregation of beta thalassemia and hereditary persistent fetal hemoglobin (Swiss type) in a Spanish family].
    De Blas JM; Martín E; Martínez ML; Caso F
    Sangre (Barc); 1985; 30(1):28-36. PubMed ID: 2408346
    [No Abstract]   [Full Text] [Related]  

  • 28. On the levels of hemoglobins F and A2 in sickle-cell anemia and some related disorders.
    Wrightstone RN; Huisman TH
    Am J Clin Pathol; 1974 Mar; 61(3):375-81. PubMed ID: 4205296
    [No Abstract]   [Full Text] [Related]  

  • 29. A new Hb variant: Hb F Sardinia gamma75(E19) isoleucine leads to threonine found in a family with Hb G Philadelphia, beta-chain deficiency and a Lepore-like haemoglobin indistinguishable from Hb A2.
    Grifoni V; Kamuzora H; Lehmann H; Charlesworth D
    Acta Haematol; 1975; 53(6):347-55. PubMed ID: 808940
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Double heterozygosity of Hb O ARAB/beta + thalassemia in an Algerian family].
    Audhuy B; North ML; Pinget M; Galacteros F; Mayer S; Dorner M
    Nouv Rev Fr Hematol (1978); 1982; 24(5):289-94. PubMed ID: 6188101
    [No Abstract]   [Full Text] [Related]  

  • 31. [Genetic study of thalassemia].
    Najean Y
    Pathol Biol; 1968 Feb; 16(3):203-8. PubMed ID: 4172570
    [No Abstract]   [Full Text] [Related]  

  • 32. Hb Lepore-Hb C and Hb Lepore-beta 0-thalassemia compound heterozygotes in an Algerian family.
    Francina A; Dorleac E; Aubry M; Baklouti F; Elwan S; Roda L; Phillipe N; Delaunay J
    Hemoglobin; 1985; 9(5):505-8. PubMed ID: 4086305
    [No Abstract]   [Full Text] [Related]  

  • 33. [Evaluation of serum ferritin in the A2 and F thalassemic syndromes].
    Mira Y; Llopis R; Cubillo P; Vayá A; Aznar J
    Sangre (Barc); 1985; 30(6):965-70. PubMed ID: 2420016
    [No Abstract]   [Full Text] [Related]  

  • 34. Molecular basis of deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia in Indian patients.
    Bhattacharya G; Banerjee D; Chandra S; Ghosh M; Chaudhuri U; Das M; Dasgupta UB
    Clin Chim Acta; 2008 Jun; 392(1-2):69-70. PubMed ID: 18343225
    [No Abstract]   [Full Text] [Related]  

  • 35. Developmental changes in hemoglobin F levels during the first two years of life in normal and heterozygous beta-thalassemia infants.
    Metaxotou-Mavromati AD; Antonopoulou HK; Laskari SS; Tsiarta HK; Ladis VA; Kattamis CA
    Pediatrics; 1982 Jun; 69(6):734-8. PubMed ID: 6176937
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Hemoglobin anomalies and medico-biological data in 10,000 Africans (author's transl)].
    Coquelet ML; Jaeger G; Mullender N
    Nouv Rev Fr Hematol (1978); 1978 Nov; 20(3):465-77. PubMed ID: 754177
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. [Double heterozygote hemoglobin D/B0 thalassemia. Report of 3 cases in a Portuguese family].
    Sousa Uva L; Fernandes A; Pilar M
    Nouv Rev Fr Hematol (1978); 1983; 25(6):387-90. PubMed ID: 6664837
    [TBL] [Abstract][Full Text] [Related]  

  • 39. F-Thalassemia. A study of thirty-one families with simple heterozygotes and combinations of F-Thalassemia with A2-Thalassemia.
    Stamatoyannopoulos G; Fessas P; Papayannopoulou T
    Am J Med; 1969 Aug; 47(2):194-208. PubMed ID: 5808240
    [No Abstract]   [Full Text] [Related]  

  • 40. Hemoglobinosis E and its association with beta-thalassemia in the Tadzhik SSR.
    Gar'kavtseva RF
    Sov Genet; 1973 Aug; 7(2):256-60. PubMed ID: 4280126
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.