BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

326 related articles for article (PubMed ID: 15339687)

  • 41. DNA diagnosis of hemoglobin mutations.
    Old JM
    Methods Mol Med; 2003; 82():101-16. PubMed ID: 12669640
    [No Abstract]   [Full Text] [Related]  

  • 42. [Thalassemia].
    Hattori Y
    Rinsho Byori; 1995 Aug; 43(8):776-80. PubMed ID: 7474435
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermedia.
    Papachatzopoulou A; Kourakli A; Makropoulou P; Kakagianne T; Sgourou A; Papadakis M; Athanassiadou A
    Eur J Haematol; 2006 Apr; 76(4):322-30. PubMed ID: 16519704
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
    Karnpean R; Fucharoen G; Fucharoen S; Sae-ung N; Sanchaisuriya K; Ratanasiri T
    Acta Haematol; 2009; 121(4):227-33. PubMed ID: 19546525
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Survey on thalassemia among people of reproductive age in Guilin City, Guangxi, China].
    Deng JY; Long AY; Li H
    Zhonghua Liu Xing Bing Xue Za Zhi; 2009 Feb; 30(2):156-8. PubMed ID: 19565877
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Detection and genetic analysis of beta-thalassemia mutations by competitive oligopriming.
    Athanassiadou A; Papachatzopoulou A; Gibbs RA
    Hum Mutat; 1995; 6(1):30-5. PubMed ID: 7550228
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Genotype-phenotype correlations in beta-thalassemias.
    Cao A; Galanello R; Rosatelli MC
    Blood Rev; 1994 Mar; 8(1):1-12. PubMed ID: 8205005
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Response to hydroxyurea therapy in beta-thalassemia.
    Koren A; Levin C; Dgany O; Kransnov T; Elhasid R; Zalman L; Palmor H; Tamary H
    Am J Hematol; 2008 May; 83(5):366-70. PubMed ID: 18181203
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Detection of alpha-thalassemia in China by using multiplex ligation-dependent probe amplification.
    Liu JZ; Han H; Schouten JP; Wang LR; Fan XP; Duarte HB; Zhu CJ; Cai R; Xiao B; Wang QT
    Hemoglobin; 2008; 32(6):561-71. PubMed ID: 19065334
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Evaluation of a single-tube multiplex polymerase chain reaction screen for detection of common alpha-thalassemia genotypes in a clinical laboratory.
    Bergstrome JA; Poon A
    Am J Clin Pathol; 2002 Jul; 118(1):18-24. PubMed ID: 12109851
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. Polymerase chain reaction-based search for two alpha-globin gene mutations in India.
    Bhattacharya G; Sarkar AA; Banerjee D; Chandra S; Das M; Dasgupta UB
    Hemoglobin; 2008; 32(5):485-90. PubMed ID: 18932074
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Coinheritance of the different copy numbers of alpha-globin gene modifies severity of beta-thalassemia/Hb E disease.
    Sripichai O; Munkongdee T; Kumkhaek C; Svasti S; Winichagoon P; Fucharoen S
    Ann Hematol; 2008 May; 87(5):375-9. PubMed ID: 18026953
    [TBL] [Abstract][Full Text] [Related]  

  • 55. High frequency of deletional alpha-thalassemia in beta-thalassemia trait: implications for genetic counseling.
    Panigrahi I; Rafeeq PH; Choudhry VP; Saxena R
    Am J Hematol; 2004 Jul; 76(3):297-9. PubMed ID: 15224373
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Co-inheritance of alpha and beta-thalassemia in a Jordanian family.
    Al Qaddoumi AA
    Clin Lab Sci; 2006; 19(3):165-8. PubMed ID: 16910233
    [TBL] [Abstract][Full Text] [Related]  

  • 57. The prevalence and molecular basis of hemoglobinopathies in Cambodia.
    Carnley BP; Prior JF; Gilbert A; Lim E; Devenish R; Sing H; Sarin E; Guhadasan R; Sullivan SG; Wise CA; Bittles AH; Chan K; Wong MS; Chan V; Erber WN
    Hemoglobin; 2006; 30(4):463-70. PubMed ID: 16987801
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Thalassemia syndromes in Saudi Arabia. Meta-analysis of local studies.
    Al-Awamy BH
    Saudi Med J; 2000 Jan; 21(1):8-17. PubMed ID: 11533744
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Study on new techniques for genetic diagnosis of deletional alpha-thalassemia].
    Liu J; Zhou J; Wang L; Zhou Y
    Zhonghua Xue Ye Xue Za Zhi; 2001 Apr; 22(4):193-6. PubMed ID: 11877072
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Detection of alpha-thalassemia-2 (-3.7 kb) and its corresponding triplication (alpha)(alpha)(alpha) (anti-3.7 kb) by PCR: an improved technical change.
    Smetanina NS; Huisman TH
    Am J Hematol; 1996 Nov; 53(3):202-3. PubMed ID: 8895694
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.