BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 16330445)

  • 1. First detection of the splice donor site IVS-I-2 (T-->B) beta-thalassemia mutation in a Chinese patient.
    Liao C; Li J; Huang Y; Li D
    Haematologica; 2005 Dec; 90(12):1695. PubMed ID: 16330445
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel beta-thalassemia trait (IVS I-1 G-->C) in a Japanese family.
    Fujihara N; Tozuka M; Ueno I; Yamauchi K; Nakagoshi R; Ishikawa S; Hirota M; Okumura N; Ishii E; Katsuyama T
    Am J Hematol; 2003 Jan; 72(1):64-6. PubMed ID: 12508270
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The codon 37 (TGG-->TAG) beta(0)-thalassemia mutation found in a Chinese family.
    Li D; Liao C; Li J; Tang X
    Hemoglobin; 2006; 30(2):171-3. PubMed ID: 16798641
    [TBL] [Abstract][Full Text] [Related]  

  • 4. BamH1 polymorphism in the Chinese, Malays, and Indians in Singapore and its application in the prenatal diagnosis of beta-thalassemia.
    Tan JA; Tay SH; Kham KY; Wong HB
    Jpn J Hum Genet; 1993 Sep; 38(3):315-8. PubMed ID: 7903173
    [TBL] [Abstract][Full Text] [Related]  

  • 5. THE Hb S/beta+ -thalassemia phenotype demonstrates that the IVS-I (-2) (A>C) mutation is a mild beta-thalassemia allele.
    Schmugge M; Waye JS; Basran RK; Zurbriggen K; Frischknecht H
    Hemoglobin; 2008; 32(3):303-7. PubMed ID: 18473247
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Genetic diagnosis of alpha and beta thalassemia dual heterozygote].
    Zeng R; Yu S; Hu B
    Zhonghua Xue Ye Xue Za Zhi; 1998 Oct; 19(10):525-7. PubMed ID: 11189497
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of a rare splice acceptor site mutation (IVS I nt 130 G-->C) of the beta globin gene in 3 patients of Eastern India.
    Bandyopadhyay A; Bandyopadhyay S; Dasgupta UB; Chandra S; Das MK
    Am J Hematol; 2001 Jun; 67(2):149. PubMed ID: 11343392
    [No Abstract]   [Full Text] [Related]  

  • 8. [A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].
    Li Q; Li LY; Mo QH
    Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jan; 28(1):16-9. PubMed ID: 18227017
    [TBL] [Abstract][Full Text] [Related]  

  • 9. First detection of the codons 41-43 (-CTTTG,+A) beta-thalassemia mutation in a Chinese patient.
    Liao C; Li DZ; Li J
    Ann Hematol; 2008 Sep; 87(9):775-6. PubMed ID: 18386005
    [No Abstract]   [Full Text] [Related]  

  • 10. Rapid detection of beta-Thalassemia alleles in Egypt using naturally or amplified created restriction sites and direct sequencing: a step in disease control.
    Hussein G; Fawzy M; Serafi TE; Ismail EF; Metwally DE; Saber MA; Giansily M; Schved JF; Pissard S; Martinez PA
    Hemoglobin; 2007; 31(1):49-62. PubMed ID: 17365005
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis based on simultaneous DNA analysis for alpha- and beta-globin genes.
    Oron-Karni V; Filon D; Rund D; Rachmilewitz E; Oppenheim A
    Am J Hematol; 1996 Nov; 53(3):203-4. PubMed ID: 8895695
    [No Abstract]   [Full Text] [Related]  

  • 12. First Detection of a Splice Acceptor Site β-Thalassemia Mutation: IVS-I-130 (HBB: c.93-1G > C) in a Chinese Patient.
    He S; Zhang Q; Zheng C; Wei Y; Tang Y; Chen Q; Chen S
    Hemoglobin; 2015; 39(4):290-1. PubMed ID: 26182339
    [TBL] [Abstract][Full Text] [Related]  

  • 13. combination of IVS2.849 A-G witH IVS1.1 G-A: a mutation of beta-globin gene in a Turkish beta-thalessemia major patient.
    Manguoğlu E; Sargin CF; Nal N; Keser I; Küpesiz A; Yeşilipek A; Lüleci G
    Pediatr Hematol Oncol; 2005 Jun; 22(4):291-5. PubMed ID: 16020116
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.
    Li D; Liao C; Li J; Xie X; Huang Y; Zhong H
    Haematologica; 2006 May; 91(5):649-51. PubMed ID: 16627247
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Diagnostic strategy of beta-thalassemic mutation in a Tunisian family, application in prenatal diagnosis].
    Khelil AH; Laradi S; Ferchichi S; Carion N; Béjaoui M; Saad A; Chaieb A; Miled A; Ben Chibani J; Perrin P
    Ann Biol Clin (Paris); 2003; 61(2):229-33. PubMed ID: 12702481
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Molecular analysis and prenatal diagnosis of beta-thalassemia: about our experience in central Tunisia].
    Laradi S; Haj Khelil A; Omri H; Chaieb A; Mahjoub T; Benlimam H; Amri F; Saad A; Miled A; Leturcq F; Ben Chibani J; Beldjord C
    Ann Biol Clin (Paris); 2000; 58(4):453-60. PubMed ID: 10932046
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A rare beta-thalassaemia mutation (C-T) at position -90 of the beta-globin gene discovered in a Chinese family.
    Jia S; Lao X; Li W; Ma J; Mo Q; Xu X
    Haematologica; 2003 Oct; 88(10):1191-3. PubMed ID: 14555318
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia.
    Chen XW; Mo QH; Li Q; Zeng R; Xu XM
    Ann Hematol; 2007 Sep; 86(9):653-7. PubMed ID: 17516066
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular mechanism of beta-thalassaemia caused by 22-bp duplication.
    Svasti S; Boonchoy C; Vanichsetakul P; Winichagoon P; Fucharoen S
    Ann Hematol; 2008 Aug; 87(8):633-7. PubMed ID: 18392622
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The rare codon 24 (T>A) (beta+) mutation in association with the common codon 39 (C> T) (beta0) mutation causes transfusion-dependent beta-thalassemia in a Moroccan patient.
    Agouti I; Bennani M; Levy N; Giordano P; Badens C
    Hemoglobin; 2009; 33(2):150-4. PubMed ID: 19373592
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.