BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 15163314)

  • 1. Molecular diagnosis of haemoglobin disorders.
    Clark BE; Thein SL
    Clin Lab Haematol; 2004 Jun; 26(3):159-76. PubMed ID: 15163314
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Screening and genetic diagnosis of haemoglobinopathies.
    Old JM
    Scand J Clin Lab Invest; 2007; 67(1):71-86. PubMed ID: 17365985
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Application of diagnostic methods and molecular diagnosis of hemoglobin disorders in Khuzestan province of Iran.
    Fakher R; Bijan K; Taghi AM
    Indian J Hum Genet; 2007 Jan; 13(1):5-15. PubMed ID: 21957335
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic predisposition to β-thalassemia and sickle cell anemia in Turkey: a molecular diagnostic approach.
    Basak AN; Tuzmen S
    Methods Mol Biol; 2011; 700():291-307. PubMed ID: 21204041
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Screening and genetic diagnosis of haemoglobin disorders.
    Old JM
    Blood Rev; 2003 Mar; 17(1):43-53. PubMed ID: 12490210
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Haemoglobinopathies.
    Old J
    Prenat Diagn; 1996 Dec; 16(13):1181-6. PubMed ID: 9061749
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China.
    Xiong F; Sun M; Zhang X; Cai R; Zhou Y; Lou J; Zeng L; Sun Q; Xiao Q; Shang X; Wei X; Zhang T; Chen P; Xu X
    Clin Genet; 2010 Aug; 78(2):139-48. PubMed ID: 20412082
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies.
    Patrinos GP; Kollia P; Papadakis MN
    Hum Mutat; 2005 Nov; 26(5):399-412. PubMed ID: 16138310
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Haemoglobin Hope in a northern Thai family: first identification of homozygous haemoglobin Hope associated with haemoglobin H disease.
    Sura T; Busabaratana M; Youngcharoen S; Wisedpanichkij R; Viprakasit V; Trachoo O
    Eur J Haematol; 2007 Sep; 79(3):251-4. PubMed ID: 17655700
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Diagnostic approach to hemoglobinopathies.
    Kutlar F
    Hemoglobin; 2007; 31(2):243-50. PubMed ID: 17486507
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Carrier screening and prenatal diagnosis of hemoglobinopathies. A study of indigenous and immigrant couples in northern Greece, over the last 5 years.
    Theodoridou S; Alemayehou M; Prappas N; Karakasidou O; Aletra V; Plata E; Tsaftaridis P; Karababa P; Boussiou M; Sinopoulou K; Hatzi A; Voskaridou E; Loutradi A; Manitsa A
    Hemoglobin; 2008; 32(5):434-9. PubMed ID: 18932067
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of hemoglobinopathies in Ontario, Canada.
    Basran RK; Patterson M; Walker L; Nakamura LM; Eng B; Chui DH; Waye JS
    Ann N Y Acad Sci; 2005; 1054():507-10. PubMed ID: 16339708
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN
    Hemoglobin; 2007; 31(2):233-41. PubMed ID: 17486506
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Student screening for inherited blood disorders in Bahrain.
    Al-Arrayed S; Hafadh N; Amin S; Al-Mukhareq H; Sanad H
    East Mediterr Health J; 2003 May; 9(3):344-52. PubMed ID: 15751927
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of the major haemoglobin disorders.
    Old JM; Thein SL; Weatherall DJ; Cao A; Loukopoulos D
    Mol Biol Med; 1989 Feb; 6(1):55-63. PubMed ID: 2666819
    [No Abstract]   [Full Text] [Related]  

  • 17. [Hemoglobinopathies in developing countries].
    Marti HR
    Wien Klin Wochenschr; 1984 Jul; 96(14):535-9. PubMed ID: 6382806
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The role of haemoglobin A(2) testing in the diagnosis of thalassaemias and related haemoglobinopathies.
    Mosca A; Paleari R; Ivaldi G; Galanello R; Giordano PC
    J Clin Pathol; 2009 Jan; 62(1):13-7. PubMed ID: 19103851
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hemoglobinopathies mimicking Hb S/beta-thalassemia: Hb S/S with alpha-thalassemia and Hb S/Volga.
    Luo HY; Heeney M; Wang WC; Eung SH; Ware RE; Steinberg MH; Chui DH
    Am J Hematol; 2006 May; 81(5):361-5. PubMed ID: 16628724
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rapid detection of fetal Mendelian disorders: thalassemia and sickle cell syndromes.
    Traeger-Synodinos J; Vrettou C; Kanavakis E
    Methods Mol Biol; 2008; 444():133-45. PubMed ID: 18425477
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.