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 *

76 related articles for article (PubMed ID: 7890938)

  • 1. Molecular pathology of thalassaemias in India.
    Misra SC; Misra RC
    J Indian Med Assoc; 1994 Nov; 92(11):353-4. PubMed ID: 7890938
    [No Abstract]   [Full Text] [Related]  

  • 2. Molecular pathology of alpha-thalassemia.
    Liebhaber SA; Kan YW
    Birth Defects Orig Artic Ser; 1982; 18(7):35-44. PubMed ID: 6760927
    [No Abstract]   [Full Text] [Related]  

  • 3. Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.
    Galanello R; Perseu L; Perra C; Maccioni L; Barella S; Longinotti M; Cao A; Cazzola M
    Br J Haematol; 2004 Dec; 127(5):604-6. PubMed ID: 15566365
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Is there an answer? The globin chain balance and imbalance.
    Vella F
    IUBMB Life; 2002 Jul; 54(1):37-8. PubMed ID: 12387574
    [No Abstract]   [Full Text] [Related]  

  • 5. Thalassemia in Ferrara.
    Vullo C
    Birth Defects Orig Artic Ser; 1982; 18(7):199-202. PubMed ID: 7159729
    [No Abstract]   [Full Text] [Related]  

  • 6. The alpha-thalassemias.
    Higgs DR; Wood WG; Jarman AP; Vickers MA; Wilkie AO; Lamb J; Vyas P; Bennett JP
    Ann N Y Acad Sci; 1990; 612():15-22. PubMed ID: 2291543
    [No Abstract]   [Full Text] [Related]  

  • 7. The alpha thalassemias.
    Orkin SH
    Tex Rep Biol Med; 1980-1981; 40():335-42. PubMed ID: 7034275
    [No Abstract]   [Full Text] [Related]  

  • 8. Silent thalassemias: genotypes and phenotypes.
    Bianco I; Cappabianca MP; Foglietta E; Lerone M; Deidda G; Morlupi L; Grisanti P; Ponzini D; Rinaldi S; Graziani B
    Haematologica; 1997; 82(3):269-80. PubMed ID: 9234571
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Compound heterozygosity of Hb D(Iran) (beta(22) Glu-->Gln) and beta(0)-thalassemia (619 bp-deletion) in India.
    Agrawal MG; Bhanushali AA; Dedhia P; Jeswani KD; Dayanand S; Dasgupta A; Das BR
    Eur J Haematol; 2007 Sep; 79(3):248-50. PubMed ID: 17655708
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Alpha thalassemia and its impact on other clinical conditions.
    Bowie LJ; Reddy PL; Beck KR
    Clin Lab Med; 1997 Mar; 17(1):97-108. PubMed ID: 9138902
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detection of a rare splice acceptor site mutation (IVS I nt 130 G-->C) of the beta globin gene in 3 patients of Eastern India.
    Bandyopadhyay A; Bandyopadhyay S; Dasgupta UB; Chandra S; Das MK
    Am J Hematol; 2001 Jun; 67(2):149. PubMed ID: 11343392
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Prenatal diagnosis of beta-thalassaemia: experience in a developing country.
    Saxena R; Jain PK; Thomas E; Verma IC
    Prenat Diagn; 1998 Jan; 18(1):1-7. PubMed ID: 9483634
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Understanding globin regulation in beta-thalassemia: it's as simple as alpha, beta, gamma, delta.
    Bank A
    J Clin Invest; 2005 Jun; 115(6):1470-3. PubMed ID: 15931385
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Overview of molecular deletion patterns of alpha0-thalassemia in Thailand.
    Wiwanitkit V
    Lab Hematol; 2004; 10(2):122-3. PubMed ID: 15224771
    [No Abstract]   [Full Text] [Related]  

  • 17. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
    Garewal G; Das R; Awasthi A; Ahluwalia J; Marwaha RK
    Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Molecular therapies in beta-thalassaemia.
    Quek L; Thein SL
    Br J Haematol; 2007 Feb; 136(3):353-65. PubMed ID: 17129232
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Candidate gene involved in genital ontogeny in chromosome region 16p13.3.
    Dame C; Albers N; Bartmann P
    Am J Med Genet; 1999 Sep; 86(3):302-3. PubMed ID: 10482886
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.