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 *

99 related articles for article (PubMed ID: 9255615)

  • 1. Hb D-Punjab in the United Arab Emirates.
    el-Kalla S; Mathews AR
    Hemoglobin; 1997 Jul; 21(4):369-75. PubMed ID: 9255615
    [No Abstract]   [Full Text] [Related]  

  • 2. Molecular basis of β-thalassemia in the United Arab Emirates.
    Baysal E
    Hemoglobin; 2011; 35(5-6):581-8. PubMed ID: 22074124
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Co-inheritance of Hb D-Punjab (codon 121; GAA-->CAA) and beta (0) -thalassemia (IVS-II-1;G-->A).
    Adekile AD; Kazanetz EG; Leonova JY; Marouf R; Khmis A; Huisman TH
    J Pediatr Hematol Oncol; 1996 May; 18(2):151-3. PubMed ID: 8846127
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel frameshift mutation causing beta-thalassemia in a Sikh.
    el-Kalla S; Mathews AR
    Hemoglobin; 1995; 19(3-4):183-9. PubMed ID: 7558874
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hb Fontainebleau (HBA2: c.64G > C) in the United Arab Emirates.
    Turner A; Sasse J; Varadi A
    Hemoglobin; 2014; 38(3):216-20. PubMed ID: 24826794
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Coinheritance of Hb D-Punjab and β-thalassemia: diagnosis and implications in prenatal diagnosis.
    Das S; Mashon RS
    Hemoglobin; 2015; 39(2):138-40. PubMed ID: 25666204
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular characterization of beta-thalassemia in the United Arab Emirates.
    el-Kalla S; Mathews AR
    Hemoglobin; 1993 Aug; 17(4):355-62. PubMed ID: 8226095
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [The association of beta zero-thalassemia and Hb D Punjab in a family of Indian origin. The second case reported in Spain].
    Ropero P; González FA; Sánchez J; Armada B; Martí E; Valdés B; Mora A; Villegas A
    Med Clin (Barc); 1997 Mar; 108(10):385-8. PubMed ID: 9139146
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hb D-Punjab [beta 121 (GH4) Glu-->Gln]/beta0-thalassemia [IVSII.1(G-->A)] in two cases from an Iranian family: first report.
    Rahimi Z; Akramipour R; Korani S; Nagel RL
    Am J Hematol; 2006 Apr; 81(4):302-3. PubMed ID: 16550524
    [No Abstract]   [Full Text] [Related]  

  • 10. Hemoglobin D/beta-thalassemia and beta-thalassemia major in a Saudi family.
    Owaidah TM; Al-Saleh MM; Al-Hellani AM
    Saudi Med J; 2005 Apr; 26(4):674-7. PubMed ID: 15900384
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A significant beta-thalassemia heterogeneity in the United Arab Emirates.
    el-Kalla S; Mathews AR
    Hemoglobin; 1997 May; 21(3):237-47. PubMed ID: 9140720
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Rare variants of Hb D Punjab, Hb O Arab and polymorphism of human hemoglobins].
    Spivak VA; Tasheva ES; Aseeva EA; Tokarev IuN
    Genetika; 1986 Mar; 22(3):511-8. PubMed ID: 3957034
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prevalence of β-thalassemia trait and abnormal hemoglobins in Sanliurfa Province in southeast Turkey.
    Incebiyik A; Genc A; Hilali NG; Camuzcuoglu A; Camuzcuoglu H; Kilic A; Vural M
    Hemoglobin; 2014; 38(6):402-4. PubMed ID: 25405917
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Misdiagnosis of Hb D-Punjab/β-thalassemia is a potential pitfall in hemoglobinopathy screening programs: a case report.
    Belhoul KM; Bakir ML; Abdulrahman M
    Hemoglobin; 2013; 37(2):119-23. PubMed ID: 23425159
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Coinheritance of HbD-Punjab/β+-thalassemia (IVSI+5 G-C) in patient with Gilbert's syndrome.
    Petrenko AA; Pivnik AV; Kim PP; Demidova EY; Surin VL; Abdullaev AO; Sudarikov AB; Petrova NA; Maryina SA
    Ter Arkh; 2018 Aug; 90(7):105-109. PubMed ID: 30701931
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hemoglobinopathy carrier prevalence in the United Arab Emirates: first analysis of the Dubai Health Authority premarital screening program results.
    Belhoul KM; Abdulrahman M; Alraei RF
    Hemoglobin; 2013; 37(4):359-68. PubMed ID: 23647352
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Presence of hemoglobinopathies in Sicily: a historic perspective.
    Schilirò G; Mirabile E; Testa R; Russo-Mancuso G; Dibenedetto SP
    Am J Med Genet; 1997 Mar; 69(2):200-6. PubMed ID: 9056562
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of beta-thalassemia mutations in the United Arab Emirates provides evidence for recurrent origin of the IVSI nt 5 (G-C) mutation.
    De Leo R; Deidda G; Novelletto A; el-Kalla S; Mathews AR; Felicetti L
    Hum Mutat; 1995; 5(4):327-8. PubMed ID: 7627187
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epidemiology of Hemoglobinopathies in the Huzhou Region, Zhejiang Province, Southeast China.
    Ding ZY; Shen GS; Zhang S; He PY
    Hemoglobin; 2016 Sep; 40(5):304-309. PubMed ID: 27615034
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of beta-thalassemia and Hb Q-Thailand resulting in a normal Hb A2 value.
    Liao C; Li J; Li D
    Hemoglobin; 2008; 32(5):505-8. PubMed ID: 18932077
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.