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 *

125 related articles for article (PubMed ID: 6172870)

  • 1. Gene deletion in hereditary persistence of fetal hemoglobin (HPFH) and delta beta thalassemia.
    Mears JG
    Tex Rep Biol Med; 1980-1981; 40():365-72. PubMed ID: 6172870
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients.
    Fucharoen S; Pengjam Y; Surapot S; Fucharoen G; Sanchaisuriya K
    Am J Hematol; 2002 Oct; 71(2):109-13. PubMed ID: 12353310
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Flow cytometric measurement of hemoglobin F in RBCs: diagnostic usefulness in the distinction of hereditary persistence of fetal hemoglobin (HPFH) and hemoglobin S-hPFH from other conditions with elevated levels of hemoglobin F.
    Hoyer JD; Penz CS; Fairbanks VF; Hanson CA; Katzmann JA
    Am J Clin Pathol; 2002 Jun; 117(6):857-63. PubMed ID: 12047136
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia.
    Wood WG; Clegg JB; Weatherall DJ
    Br J Haematol; 1979 Dec; 43(4):509-20. PubMed ID: 93487
    [No Abstract]   [Full Text] [Related]  

  • 7. Molecular characterization of delta beta-thalassemia and hereditary persistence of fetal hemoglobin in the Indian population.
    Nadkarni A; Wadia M; Gorakshakar A; Kiyama R; Colah RB; Mohanty D
    Hemoglobin; 2008; 32(5):425-33. PubMed ID: 18932066
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Restriction endonuclease gene mapping studies of an Indian (A gamma delta beta)zero-thalassaemia, previously identified as G gamma-HPFH.
    Nakatsuji T; Gilman JG; Sukumaran PK; Huisman TH
    Br J Haematol; 1984 Aug; 57(4):663-70. PubMed ID: 6204682
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Compound heterozygote state for GgammaAgamma(deltabeta) degrees -thalassemia and hereditary persistence of fetal hemoglobin.
    Fucharoen S; Panyasai S; Surapot S; Fucharoen G; Sanchaisuriya K
    Am J Hematol; 2005 Oct; 80(2):119-23. PubMed ID: 16184575
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man.
    Tuan D; Feingold E; Newman M; Weissman SM; Forget BG
    Proc Natl Acad Sci U S A; 1983 Nov; 80(22):6937-41. PubMed ID: 6196781
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A conserved gene 3' to the HPFH-1 deletion breakpoint may have an effect on fetal globin gene expression in HPFH-1.
    Penny LA; Forget BG
    Prog Clin Biol Res; 1989; 316B():133-41. PubMed ID: 2482494
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Molecular studies of mutations that increase Hb F production in man.
    Forget BG; Tuan D; Newman MV; Feingold EA; Collins F; Fukumaki Y; Jagadeeswaran P; Weissman SM
    Prog Clin Biol Res; 1983; 134():65-76. PubMed ID: 6198666
    [No Abstract]   [Full Text] [Related]  

  • 14. [Molecular-genetic characteristics of alpha, beta and delta beta-thalassemias in 139 heterozygotes in 56 unrelated Czech and Slovak families (Priority description of 3 beta-thalassemia mutations, an extensive alpha-thalassemia 2 (18+ kb) deletion and a Swiss-type nondeletion hereditary persistence of hemoglobin F)].
    Indrák K; Divoký V; Brabec V; Indráková J; Svobodová M; Huisman TH
    Vnitr Lek; 1993 Oct; 39(10):969-78. PubMed ID: 7694425
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular characterization and hematological phenotype of Sicilian delta beta-thalassemia .
    Camaschella C; Serra A; Bertero MT; Trento M; Dall'Acqua M; Gottardi E; Izzo P; Brancati C; Mazza U
    Haematologica; 1986; 71(4):287-92. PubMed ID: 2430864
    [No Abstract]   [Full Text] [Related]  

  • 16. The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobases.
    Camaschella C; Serra A; Saglio G; Baiget M; Malgaretti N; Mantovani R; Ottolenghi S
    Blood; 1987 Aug; 70(2):593-6. PubMed ID: 2440503
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. High Hb F levels in a Sardinian family: a genetic defect intermediate between HPFH Greek type and delta beta-thalassemia?
    David O; Miniero R; Sacchetti L; Cappellini MD; Giglioni B; Comi P; Ottolenghi S; Saglio G; Guerrasio A; Camaschella C; Mazza U
    Haematologica; 1982 Aug; 67(4):499-507. PubMed ID: 6183172
    [No Abstract]   [Full Text] [Related]  

  • 19. Molecular characterisation of Vietnamese HPFH.
    Motum PI; Hamilton TJ; Lindeman R; Le H; Trent RJ
    Hum Mutat; 1993; 2(3):179-84. PubMed ID: 7689901
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unusual combination of genetic defects in a Sicilian boy: G gamma delta beta thalassemia, G gamma A gamma heterocellular HPFH, beta (0) thalassemia, and albinism.
    Schilirò G; Pavone L; Romeo MA; Russo A; Musumeci S; Russo G
    Am J Med Genet; 1983 Jun; 15(2):225-31. PubMed ID: 6192718
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.