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 *

171 related articles for article (PubMed ID: 12792697)

  • 1. Thalassemia intermedia as a result of heterozygosis for beta 0 -thalassemia and alpha alpha alpha anti-3,7 genotype in a Brazilian patient.
    Kimura EM; Grignoli CR; Pinheiro VR; Costa FF; Sonati MF
    Braz J Med Biol Res; 2003 Jun; 36(6):699-701. PubMed ID: 12792697
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Heterozygous β thalassemia with triplication of the α globin gene].
    Constanço MC; Rocha P; Bento C; Silva HM
    Acta Med Port; 2011; 24(4):633-6. PubMed ID: 22521023
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Thalassemia intermedia caused by interaction of IVS-1 1(G--A) mutation in the beta-globin gene and heterozygotic triplication in the alpha-globin gene].
    Martínez-López J; Galán García P; del Río E; Baiget M; Gilsanz Rodríguez F
    Rev Clin Esp; 1998 Mar; 198(3):153-5. PubMed ID: 9586437
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patients.
    Harteveld CL; Refaldi C; Cassinerio E; Cappellini MD; Giordano PC
    Blood Cells Mol Dis; 2008; 40(3):312-6. PubMed ID: 18249014
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Molecular diagnosis in a Korean family with thalassemia intermedia due to co-inheritance of triplicated alpha-globin genes (alphaalpha/alphaalphaalpha(anti 3.7)) and beta-thalassemia trait (IVS-II-1 G-->A)].
    Chen M; Han JY; Sun Q; Kim IH; Ren Z; Huang S; Zeng Y
    Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):195-7. PubMed ID: 11876981
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genes.
    Mehta PR; Upadhye DS; Sawant PM; Gorivale MS; Nadkarni AH; Shanmukhaiah C; Ghosh K; Colah RB
    Ann Hematol; 2015 Dec; 94(12):1953-8. PubMed ID: 26319530
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia.
    Farashi S; Bayat N; Faramarzi Garous N; Ashki M; Montajabi Niat M; Vakili S; Imanian H; Zeinali S; Najmabadi H; Azarkeivan A
    Hemoglobin; 2015; 39(3):201-6. PubMed ID: 26084319
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia.
    Rhodes SL; Plonczynski M; Harrell A; Li J; Safaya S; Files JC; Steinberg MH
    Am J Med Sci; 1999 May; 317(5):341-5. PubMed ID: 10334122
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of an α-globin gene cluster duplication and heterozygous β-thalassemia in a patient with a severe thalassemia syndrome.
    Jiang H; Liu S; Zhang YL; Wan JH; Li R; Li DZ
    Hemoglobin; 2015; 39(2):102-6. PubMed ID: 25690803
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Case report: Identification of a novel triplication of alpha-globin gene by the third-generation sequencing: pedigree analysis and genetic diagnosis.
    Chen Y; Xie T; Ma M; Yang J; Lv Y; Dong X
    Hematology; 2023 Dec; 28(1):2277571. PubMed ID: 38059617
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Moderate reduction of beta-globin gene transcript by a novel mutation in the 5' untranslated region: a study of its interaction with other genotypes in two families.
    Ho PJ; Rochette J; Fisher CA; Wonke B; Jarvis MK; Yardumian A; Thein SL
    Blood; 1996 Feb; 87(3):1170-8. PubMed ID: 8562944
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM; El-Khatib FF; Ayesh S
    Hemoglobin; 2005; 29(2):119-32. PubMed ID: 15921164
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comparative in vivo expression of beta(+)-thalassemia alleles.
    Marwan MM; Scerri CA; Zarroag SO; Cao A; Kyrri A; Kalogirou E; Kleanthous M; Ioannou P; Angastiniotis M; Felice AE
    Hemoglobin; 1999 Aug; 23(3):221-9. PubMed ID: 10490134
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic analysis of beta-thalassemia intermedia in Israel: diversity of mechanisms and unpredictability of phenotype.
    Rund D; Oron-Karni V; Filon D; Goldfarb A; Rachmilewitz E; Oppenheim A
    Am J Hematol; 1997 Jan; 54(1):16-22. PubMed ID: 8980256
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Severe thalassaemia intermedia caused by interaction of homozygosity for alpha-globin gene triplication with heterozygosity for beta zero-thalassaemia.
    Oron V; Filon D; Oppenheim A; Rund D
    Br J Haematol; 1994 Feb; 86(2):377-9. PubMed ID: 8199028
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenotypes of individuals with a beta thal classical allele associated either with a beta thal silent allele or with alpha globin gene triplication.
    Bianco I; Lerone M; Foglietta E; Deidda G; Cappabianca MP; Morlupi L; Ponzini D; Grisanti P; Di Biagio P; Amato A; Mezzabotta M; Graziani B
    Haematologica; 1997; 82(5):513-25. PubMed ID: 9407714
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular mechanisms underlying thalassemia intermedia in Iran.
    Neishabury M; Azarkeivan A; Oberkanins C; Esteghamat F; Amirizadeh N; Najmabadi H
    Genet Test; 2008 Dec; 12(4):549-56. PubMed ID: 18939939
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Molecular diagnosis of beta-thalassemia intermedia].
    Chen J; Liu W; Chen M
    Zhonghua Yi Xue Za Zhi; 1997 Aug; 77(8):575-8. PubMed ID: 9772460
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia.
    Vinciguerra M; Passarello C; Cassarà F; Leto F; Cannata M; Calvaruso G; Di Maggio R; Renda D; Maggio A; Giambona A
    Int J Lab Hematol; 2016 Feb; 38(1):17-26. PubMed ID: 26418075
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.