BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

101 related articles for article (PubMed ID: 24145931)

  • 1. Advanced techniques in molecular genetics and its implications on genetic testing and screening in the Arabian Peninsula.
    Abu-Amero KK; Kondkar AA
    Saudi Med J; 2013 Oct; 34(10):995-1001. PubMed ID: 24145931
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A new era for preventive genetic programs in the Arabian Peninsula.
    Al-Odaib AN; Abu-Amero KK; Ozand PT; Al-Hellani AM
    Saudi Med J; 2003 Nov; 24(11):1168-75. PubMed ID: 14647548
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Commercial molecular diagnostics in the U.S.: The Human Genome Project to the clinical laboratory.
    Amos J; Patnaik M
    Hum Mutat; 2002 Apr; 19(4):324-33. PubMed ID: 11933187
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recent advances in the molecular genetics of epilepsy.
    Hildebrand MS; Dahl HH; Damiano JA; Smith RJ; Scheffer IE; Berkovic SF
    J Med Genet; 2013 May; 50(5):271-9. PubMed ID: 23468209
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detection and interpretation of genomic structural variation in health and disease.
    Vandeweyer G; Kooy RF
    Expert Rev Mol Diagn; 2013 Jan; 13(1):61-82. PubMed ID: 23256704
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Basics of molecular biology and its applications: I. Molecular biology in medicine: basic concepts.
    Erasmus RT; Murthy DP; Ogunbanjo BO
    P N G Med J; 1996 Mar; 39(1):56-66. PubMed ID: 9522852
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genome-wide arrays in routine diagnostics of hematological malignancies.
    Simons A; Sikkema-Raddatz B; de Leeuw N; Konrad NC; Hastings RJ; Schoumans J
    Hum Mutat; 2012 Jun; 33(6):941-8. PubMed ID: 22488943
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Gene technology in clinical medicine--technics and tools].
    Børresen AL
    Tidsskr Nor Laegeforen; 1989 Oct; 109(28):2882-7. PubMed ID: 2815027
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Strategies for the prevention of hereditary diseases in a highly consanguineous population.
    Meyer BF
    Ann Hum Biol; 2005; 32(2):174-9. PubMed ID: 16096214
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Testing environment for single-gene disorders in U.S. reference laboratories.
    Amos J; Gold B
    Hum Mutat; 1998; 12(5):293-300. PubMed ID: 9792404
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetics of neuromuscular disorders.
    Laing NG
    Crit Rev Clin Lab Sci; 2012; 49(2):33-48. PubMed ID: 22468856
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetics and DNA technology.
    Arzimanoglou II; Gilbert F
    Curr Opin Obstet Gynecol; 1994 Oct; 6(5):445-52. PubMed ID: 7827276
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic testing considerations for oral medicine.
    Hart TC; Ferrell RE
    J Dent Educ; 2002 Oct; 66(10):1185-202. PubMed ID: 12449214
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical genotyping: the need for interrogation of single nucleotide polymorphisms and mutations in the clinical laboratory.
    Tsongalis GJ; Coleman WB
    Clin Chim Acta; 2006 Jan; 363(1-2):127-37. PubMed ID: 16102741
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Knowledge and attitude toward the hemoglobinopathies premarital screening program in Saudi Arabia: population-based survey.
    Al Sulaiman A; Suliman A; Al Mishari M; Al Sawadi A; Owaidah TM
    Hemoglobin; 2008; 32(6):531-8. PubMed ID: 19065330
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Impact of new genomic tools on the practice of clinical genetics in consanguineous populations: the Saudi experience.
    Alkuraya FS
    Clin Genet; 2013 Sep; 84(3):203-8. PubMed ID: 23451714
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Microelectronic array system for molecular diagnostic genotyping: Nanogen NanoChip 400 and molecular biology workstation.
    Keen-Kim D; Grody WW; Richards CS
    Expert Rev Mol Diagn; 2006 May; 6(3):287-94. PubMed ID: 16706733
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The phenotype of a CASQ2 mutation in a Saudi family with catecholaminergic polymorphic ventricular tachycardia.
    Al-Hassnan ZN; Tulbah S; Al-Manea W; Al-Fayyadh M
    Pacing Clin Electrophysiol; 2013 May; 36(5):e140-2. PubMed ID: 22650415
    [TBL] [Abstract][Full Text] [Related]  

  • 19. T313M PINK1 mutation in an extended highly consanguineous Saudi family with early-onset Parkinson disease.
    Chishti MA; Bohlega S; Ahmed M; Loualich A; Carroll P; Sato C; St George-Hyslop P; Westaway D; Rogaeva E
    Arch Neurol; 2006 Oct; 63(10):1483-5. PubMed ID: 17030667
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cell-free fetal nucleic acid testing: a review of the technology and its applications.
    Sayres LC; Cho MK
    Obstet Gynecol Surv; 2011 Jul; 66(7):431-42. PubMed ID: 21944155
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.