BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

28 related articles for article (PubMed ID: 10228390)

  • 1. Reciprocal and nonreciprocal recombination at the glucocerebrosidase gene region: implications for complexity in Gaucher disease.
    Tayebi N; Stubblefield BK; Park JK; Orvisky E; Walker JM; LaMarca ME; Sidransky E
    Am J Hum Genet; 2003 Mar; 72(3):519-34. PubMed ID: 12587096
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dominantly Inherited beta-Thalassemia.
    Efremov GD
    Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular mechanisms of thalassemia in southeast Asia.
    Winichagoon P; Fucharoen S; Wilairat P; Fukumaki Y
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():235-40. PubMed ID: 8629113
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular epidemiological study of alpha- and beta-thalassemia in Sihui city.
    Tan JR; Li WJ; Ma JY; Mo QH; Li LY; Jia SQ; Lao XW; Li LY; He RQ; Xu XM
    Di Yi Jun Yi Da Xue Xue Bao; 2003 Jul; 23(7):716-9. PubMed ID: 12865230
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
    Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E
    Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new insertion mutation in the beta-globin gene [codons 45/46 (+A)] resulting in a beta-thalassemia minor phenotype.
    Cornut G; Weng X; Robin L; Lavoie C; Marchand S; Soulières D
    Hemoglobin; 2007; 31(3):393-5. PubMed ID: 17654079
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Globin gene mutation is a model of genetic abnormalities].
    Hattori Y
    Rinsho Byori; 1999 Mar; 47(3):244-51. PubMed ID: 10228390
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia.
    Wajcman H; Traeger-Synodinos J; Papassotiriou I; Giordano PC; Harteveld CL; Baudin-Creuza V; Old J
    Hemoglobin; 2008; 32(4):327-49. PubMed ID: 18654884
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Human globin genes: what can we learn from their polymorphism?].
    Charmot-Bensimon D
    Bull Soc Pathol Exot; 1999; 92(4):242-8. PubMed ID: 10572659
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular nature of alpha-globin genes in the Saudi population.
    Borgio JF
    Saudi Med J; 2015 Nov; 36(11):1271-6. PubMed ID: 26593158
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Congenital hemolytic anemia--hemoglobin abnormality--thalassemia].
    Fujita S
    Nihon Rinsho; 1996 Sep; 54(9):2454-9. PubMed ID: 8890578
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Thalassemia mutations and their clinical aspects in Japan.
    Hattori Y
    Int J Hematol; 2002 Aug; 76 Suppl 2():90-2. PubMed ID: 12430906
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 14.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 15.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 16.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 17.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 2.