These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 19125249)

  • 1. A novel beta-thalassemic allele due to a thirteen nucleotide deletion: codons 54-58 (-T ATG GGC AAC CCT).
    Li DZ; Liao C; Li J
    Ann Hematol; 2009 Aug; 88(8):799-801. PubMed ID: 19125249
    [No Abstract]   [Full Text] [Related]  

  • 2. Detection of a rare mutation in an Iranian family: codons 37/38/39 (7 bp deletion).
    Zadeh-Vakili A; Eshghi P
    Hemoglobin; 2009; 33(6):523-7. PubMed ID: 19958201
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian population.
    Nadkarni A; Gorakshakar A; Surve R; Sawant P; Phanasgaonkar S; Nair S; Ghosh K; Colah RB
    Hemoglobin; 2009; 33(1):59-65. PubMed ID: 19205975
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A family with the 619 bp deletion on the beta-globin gene found in Kerman Province, Iran.
    Saleh-Gohari N; Mashizi AK
    Hemoglobin; 2009; 33(6):515-8. PubMed ID: 19958199
    [TBL] [Abstract][Full Text] [Related]  

  • 5. beta-Thalassemia mutations in the Iranian Kurdish population of Kurdistan and West Azerbaijan provinces.
    Haghi M; Khorshidi S; Hosseinpour Feizi MA; Pouladi N; Hosseinpour Feizi AA
    Hemoglobin; 2009; 33(2):109-14. PubMed ID: 19373586
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of unknown deletions in beta-globin gene cluster using PCR-reverse dot-blot method in prenatal diagnosis.
    Liao C; Li DZ
    Eur J Haematol; 2009 Oct; 83(4):385-6. PubMed ID: 19519729
    [No Abstract]   [Full Text] [Related]  

  • 7. Severe β-thalassemia intermedia in a compound heterozygous patient for the -30 (T>A) β(+)-thalassemia mutation and the δ(0)β(+)-Senegalese deletion.
    Griffon C; Joly P; Sénéchal A; Philit F; Francina A
    Hemoglobin; 2010; 34(5):505-8. PubMed ID: 20854126
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A novel mutation of -50 (G-->A) in the direct repeat element of the beta-globin gene identified in a patient with severe beta-thalassemia.
    Li DZ; Liao C; Xie XM; Zhou JY
    Ann Hematol; 2009 Nov; 88(11):1149-50. PubMed ID: 19290524
    [No Abstract]   [Full Text] [Related]  

  • 10. A novel deletional beta-thalassemic variant in an ethnic Qatari patient.
    Al-Obaidli A; Gerard N; Al Zadjali S; Fawzi Z; Pravin S; Pathare A; Krishnamoorthy R
    Hemoglobin; 2009; 33(3):214-9. PubMed ID: 19657835
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The importance of β globin deletion analysis in the evaluation of patients with β thalassemia.
    Mikula M; Buller-Burckle A; Gallivan M; Sun W; Franklin CR; Strom CM
    Int J Lab Hematol; 2011 Jun; 33(3):310-7. PubMed ID: 21219590
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Preimplantation genetic diagnosis for beta-thalassemia using single-cell DNA analysis for codons 17 and 26 of beta-globin gene.
    Nasri NW; Jamal AR; Abdullah NC; Razi ZR; Mokhtar NM
    Arch Med Res; 2009 Jan; 40(1):1-9. PubMed ID: 19064120
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Application of maternal plasma DNA analysis for noninvasive prenatal diagnosis of Hb E-beta-thalassemia.
    Tungwiwat W; Fucharoen G; Fucharoen S; Ratanasiri T; Sanchaisuriya K; Sae-Ung N
    Transl Res; 2007 Nov; 150(5):319-25. PubMed ID: 17964521
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two new beta0-thalassemic mutations: a deletion (-CC) at codon 142 or overlapping codons 142-143, and an insertion (+T) at codon 45 or overlapping codons 44-45/45-46 of the beta-globin gene.
    Lacan P; Aubry M; Couprie N; Francina A
    Hemoglobin; 2007; 31(2):159-65. PubMed ID: 17486497
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Homozygosity for a rare beta 0-thalassemia mutation [frameshift codons 25/26 (+T)] causes beta-thalassemia intermedia in an Iranian family.
    Haghi M; Feizi AA; Harteveld CL; Pouladi N; Feizi MA
    Hemoglobin; 2009; 33(1):75-80. PubMed ID: 19205978
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of beta-thalassemia/Hb E by hemoglobin typing compared to DNA analysis.
    Sirichotiyakul S; Saetung R; Sanguansermsri T
    Hemoglobin; 2009; 33(1):17-23. PubMed ID: 19205969
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The 4-bp deletion (-AAAC) in the 5' untranslated region of the beta-globin gene: a simple polymorphism?
    Li DZ; Liao C; Li J; Xie XM; Zhong HZ
    Ann Hematol; 2009 Jul; 88(7):709-10. PubMed ID: 19066892
    [No Abstract]   [Full Text] [Related]  

  • 20. A novel beta-Thalassemic allele due to a two nucleotide deletion: beta76 (-GC).
    Foulon K; Rochette J; Cadet E
    Hemoglobin; 2007; 31(1):31-7. PubMed ID: 17365003
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.