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 *

356 related articles for article (PubMed ID: 1694572)

  • 1. Hemoglobin Bart's disease in an Italian boy. Interaction between alpha-thalassemia and hereditary persistence of fetal hemoglobin.
    Chui DH; Patterson M; Dowling CE; Kazazian HH; Kendall AG
    N Engl J Med; 1990 Jul; 323(3):179-82. PubMed ID: 1694572
    [No Abstract]   [Full Text] [Related]  

  • 2. [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]  

  • 3. A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the beta-globin gene complex.
    Thein SL; Weatherall DJ
    Prog Clin Biol Res; 1989; 316B():97-111. PubMed ID: 2482508
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia.
    Kalamaras A; Chassanidis C; Samara M; Papadakis MN; Vagena A; Aleporou-Marinou V; Patrinos GP; Kollia P
    Am J Hematol; 2008 Sep; 83(9):760. PubMed ID: 18615450
    [No Abstract]   [Full Text] [Related]  

  • 6. Mutations in the A gamma-globin promoter in hereditary persistence of fetal hemoglobin and delta beta zero-thalassemia.
    Ottolenghi S; Giglioni B; Comi P; Mantovani R; Malgaretti N; Nicolis S; Longinotti M; Sciarratta GV; Pirastu M; Camaschella C
    Prog Clin Biol Res; 1987; 251():373-82. PubMed ID: 2448807
    [No Abstract]   [Full Text] [Related]  

  • 7. [Genetic and hematological study of a family from Ghana suffering from hereditary persistence of fetal hemoglobin associated with beta-thalassemia and hemoglobinosis S].
    Boreux G; Wyss M; Farquet JJ
    Arch Genet (Zur); 1973; 46(1):22-33. PubMed ID: 4731929
    [No Abstract]   [Full Text] [Related]  

  • 8. Delta beta thalassemia and hereditary persistence of fetal hemoglobin.
    Bollekens JA; Forget BG
    Hematol Oncol Clin North Am; 1991 Jun; 5(3):399-422. PubMed ID: 1713909
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
    Panyasai S; Fucharoen S; Surapot S; Fucharoen G; Sanchaisuriya K
    Haematologica; 2004 Jul; 89(7):777-81. PubMed ID: 15257928
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heterogeneity of molecular defects underlying hereditary persistence of fetal hemoglobin in Mediterranean area.
    Ottolenghi S; Giglioni B; Casini C; Merli S; Mantovani R; Comi P; Serra A; Guerrasio A; Camaschella C; Saglio G
    Prog Clin Biol Res; 1985; 191():151-61. PubMed ID: 2413471
    [No Abstract]   [Full Text] [Related]  

  • 11. Studies of hemoglobin Bart and deletion of alpha-globin genes from cord blood in Thailand.
    Tanphaichitr VS; Pung-amritt P; Puchaiwatananon O; Winichagoon P; Fucharoen S; Suvatte V; Wasi P
    Birth Defects Orig Artic Ser; 1987; 23(5A):15-21. PubMed ID: 2825828
    [No Abstract]   [Full Text] [Related]  

  • 12. Total deletion of alpha-globin genes in 2 cases of hemoglobin Bart's hydrops fetalis.
    Ko TM; Lee SC; Hsieh FJ; Lee TY; Lin JK
    Taiwan Yi Xue Hui Za Zhi; 1986 Jun; 85(6):624-9. PubMed ID: 3463666
    [No Abstract]   [Full Text] [Related]  

  • 13. delta beta-Thalassemia and HPFH.
    Ottolenghi S; Giglioni B; Taramelli R; Comi P; Gianni AM
    Birth Defects Orig Artic Ser; 1982; 18(7):65-7. PubMed ID: 6186314
    [No Abstract]   [Full Text] [Related]  

  • 14. Deletion and non deletion hereditary persistence of fetal hemoglobin in Italy.
    Camaschella C; Serra A; Alfarano A; Gottardi E; Revello D; Bertero MT; Oggiano L; Longinotti M; Saglio G
    Haematologica; 1990; 75 Suppl 5():26-30. PubMed ID: 1707848
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Neonatal screening for Hb Bart's in Italian subjects of heterogeneous regional origin born in Lombardy.
    Velati C; Sampietro M; Sciariada L; Allievi E; Mosconi L; Cappellini MD; Fiorelli G
    Haematologica; 1983; 68(1):20-9. PubMed ID: 6188651
    [No Abstract]   [Full Text] [Related]  

  • 17. Alpha thalassaemia in an Italian population.
    Velati C; Sampietro M; Biassoni M; Cappellini MD; Wainscoat JS; Higgs DR; Fiorelli G
    Br J Haematol; 1986 Jul; 63(3):497-501. PubMed ID: 3755350
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Heterozygous beta-thalassemia without icrease of hemoglobin A2].
    Marti HR; Grieder HR
    Schweiz Med Wochenschr; 1970 Apr; 100(15):663-6. PubMed ID: 5438669
    [No Abstract]   [Full Text] [Related]  

  • 19. Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.
    Tan J; Tay JS; Wong YC; Kham SK; Bte Abd Aziz N; Teo SH; Wong HB
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():252-6. PubMed ID: 8629117
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Kenya haemoglobin.
    Kendall AG; Ojwang PJ
    East Afr Med J; 1974 Jun; 51(6):434-43. PubMed ID: 4425520
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 18.