BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

90 related articles for article (PubMed ID: 20704537)

  • 1. ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia.
    Shammas C; Papasavva T; Felekis X; Christophorou C; Roomere H; Synodinos JT; Kanavakis E; El-Khateeb M; Hamamy H; Mahmoud T; Shboul M; El Beshlawy A; Filon D; Hussein IR; Galanello R; Romeo G; Kleanthous M
    Clin Chem Lab Med; 2010 Dec; 48(12):1713-8. PubMed ID: 20704537
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Single nucleotide polymorphisms of β-globin gene in β-thalassaemia patients].
    Sun SC; Cao JH; Guo L; Peng YS; He JB
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Oct; 18(5):1220-3. PubMed ID: 21129264
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The use of Taqman genotyping assays for rapid confirmation of β-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations.
    Teh LK; Lee TY; Tan JA; Lai MI; George E
    Int J Lab Hematol; 2015 Feb; 37(1):79-89. PubMed ID: 24725998
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of three new nucleotide substitutions in the β-globin gene: laboratoristic approach and impact on genetic counselling for beta-thalassaemia.
    Vinciguerra M; Passarello C; Leto F; Cassarà F; Cannata M; Maggio A; Giambona A
    Eur J Haematol; 2014; 92(5):444-9. PubMed ID: 24401016
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Development of a High-Resolution Melting Approach for Scanning Beta Globin Gene Point Mutations in the Greek and Other Mediterranean Populations.
    Chassanidis C; Boutou E; Voskaridou E; Balassopoulou A
    PLoS One; 2016; 11(6):e0157393. PubMed ID: 27351925
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Improved hybridization probe method for genetic analysis of beta-thalassemia].
    Yamashiro Y; Hattori Y; Hino M; Furuya C; Fukamitu A; Suehisa Y
    Rinsho Byori; 2011 Sep; 59(9):858-63. PubMed ID: 22111303
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A minimal set of SNPs for the noninvasive prenatal diagnosis of β-thalassaemia.
    Papasavva TE; Lederer CW; Traeger-Synodinos J; Mavrou A; Kanavakis E; Ioannou C; Makariou C; Kleanthous M
    Ann Hum Genet; 2013 Mar; 77(2):115-24. PubMed ID: 23362932
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An overview of current microarray-based human globin gene mutation detection methods.
    Cremonesi L; Ferrari M; Giordano PC; Harteveld CL; Kleanthous M; Papasavva T; Patrinos GP; Traeger-Synodinos J
    Hemoglobin; 2007; 31(3):289-311. PubMed ID: 17654067
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Noninvasive prenatal diagnostic assay for the detection of beta-thalassemia.
    Papasavva T; Kalakoutis G; Kalikas I; Neokli E; Papacharalambous S; Kyrri A; Kleanthous M
    Ann N Y Acad Sci; 2006 Sep; 1075():148-53. PubMed ID: 17108205
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genotyping of β-globin gene mutations in single lymphocytes: a preliminary study for preimplantation genetic diagnosis of monogenic disorders.
    Durmaz B; Ozkinay F; Onay H; Karaca E; Aydinok Y; Tavmergen E; Vrettou C; Traeger-Synodinos J; Kanavakis E
    Hemoglobin; 2012; 36(3):230-43. PubMed ID: 22524255
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutational Analysis Of Beta Thalassaemia By Multiplex Arms-Pcr In Khyber Pakhtunkhwa, Pakistan.
    Jalil T; Yousafzai YM; Rashid I; Ahmed S; Ali A; Fatima S; Ahmed J
    J Ayub Med Coll Abbottabad; 2019; 31(1):98-103. PubMed ID: 30868793
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Comprehensive and efficient HBB mutation analysis for detection of beta-hemoglobinopathies in a pan-ethnic population.
    Chan OT; Westover KD; Dietz L; Zehnder JL; Schrijver I
    Am J Clin Pathol; 2010 May; 133(5):700-7. PubMed ID: 20395516
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Testing for haemoglobinopathies in Johannesburg, South Africa: a 30-year review.
    Krause A; Wainstein T; Essop FB; Goodyear Q
    S Afr Med J; 2013 Oct; 103(12 Suppl 1):989-93. PubMed ID: 24300645
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prevalence of β-Thalassemia and hemoglobin E in two migrant populations of Manipur, North East India.
    Achoubi N; Asghar M; Saraswathy KN; Murry B
    Genet Test Mol Biomarkers; 2012 Oct; 16(10):1195-200. PubMed ID: 23057593
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of beta-globin gene mutations among Kelantan Malay thalassaemia patients by polymerase chain reaction restriction fragment length polymorphism.
    Rozitah R; Nizam MZ; Nur Shafawati AR; Nor Atifah MA; Dewi M; Kannan TP; Ariffin N; Norsarwany M; Setianingsih I; Harahap A; Zilfalil BA
    Singapore Med J; 2008 Dec; 49(12):1046-9. PubMed ID: 19122960
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel β-globin gene mutation HBB.c.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC.
    Edison ES; Sathya M; Rajkumar SV; Nair SC; Srivastava A; Shaji RV
    Int J Lab Hematol; 2012 Oct; 34(5):556-8. PubMed ID: 22471768
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genotype of thalassemia genes and the polymorphism of β- globin gene in Cantonese].
    Liu L; Jiang WY; Xu SY; Chen J; Chen LM; Tian QH; Wang JC
    Zhonghua Xue Ye Xue Za Zhi; 2013 Jul; 34(7):595-9. PubMed ID: 23906453
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Arrayed primer extension for the noninvasive prenatal diagnosis of beta-thalassemia based on detection of single nucleotide polymorphisms.
    Papasavva T; Kalikas I; Kyrri A; Kleanthous M
    Ann N Y Acad Sci; 2008 Aug; 1137():302-8. PubMed ID: 18837964
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spatially addressable bead-based biosensor for rapid detection of beta-thalassemia mutations.
    Ng JK; Wang W; Liu WT; Chong SS
    Anal Chim Acta; 2010 Jan; 658(2):193-6. PubMed ID: 20103094
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A comprehensive scanning method for rapid detection of beta-globin gene mutations and polymorphisms.
    Ghanem N; Girodon E; Vidaud M; Martin J; Fanen P; Plassa F; Goossens M
    Hum Mutat; 1992; 1(3):229-39. PubMed ID: 1301930
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.