BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

20 related articles for article (PubMed ID: 24261598)

  • 1. [Cases Analysis of Hemoglobin H Disease Caused by
    Wang QH; Chen XY; Tang N; Yan TZ; Huang J; Zhong QY; Luo SQ
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2024 Apr; 32(2):520-524. PubMed ID: 38660861
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (AT
    Lei YL; Sui H; Liu YJ; Pan JJ; Liu YH; Lou JW
    Hemoglobin; 2019; 43(4-5):241-244. PubMed ID: 31690131
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Targeted next-generation sequencing of the ATP7B gene for molecular diagnosis of Wilson disease.
    Poon KS; Tan KM; Koay ES
    Clin Biochem; 2016 Jan; 49(1-2):166-71. PubMed ID: 26483271
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (
    Du L; Bao X; He W; Qin D; Wang J; Xiong Y; Shi X; Ding H; Yao C; Wu J
    J Int Med Res; 2021 Jul; 49(7):3000605211031429. PubMed ID: 34334003
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Iranian patients with hemoglobin H disease: genotype-phenotype correlation.
    Paridar M; Azizi E; Keikhaei B; Takhviji V; Baluchi I; Khosravi A
    Mol Biol Rep; 2019 Oct; 46(5):5041-5048. PubMed ID: 31273613
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of Hb H disease genotypes common in northern Thailand by quantitative real-time polymerase chain reaction and high resolution melting analyses.
    Seeratanachot T; Sanguansermsri T; Shimbhu D
    Hemoglobin; 2013; 37(6):574-83. PubMed ID: 23957826
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hb H Hydrops Fetalis Syndrome Caused by Association of the - -(SEA) Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family.
    He S; Zheng C; Meng D; Chen R; Zhang Q; Tian X; Chen S
    Hemoglobin; 2015; 39(3):216-9. PubMed ID: 25897478
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspects.
    Fucharoen S; Fucharoen G
    Hemoglobin; 2012; 36(1):18-24. PubMed ID: 22145566
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (- -
    Yang X; Yan JM; Li J; Xie XM; Zhou JY; Li Y; Li DZ
    Hemoglobin; 2016 Sep; 40(5):353-355. PubMed ID: 27686733
    [TBL] [Abstract][Full Text] [Related]  

  • 10. First Case of a Compound Heterozygosity for Two Nondeletional α-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze.
    Zhou JY; Yan JM; Li J; Li DZ
    Hemoglobin; 2016 Jun; 40(3):210-2. PubMed ID: 26956449
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Hb H disease genotypes in Southern China.
    Fang J; Chen L; Zeng R; Tian Q; Jiang W; Li H; Chen Z; Du C; Chen S
    Hemoglobin; 2014; 38(1):76-8. PubMed ID: 24261598
    [TBL] [Abstract][Full Text] [Related]  

  • 12.
    ; ; . PubMed ID:
    [No 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 1.