BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

938 related articles for article (PubMed ID: 12210807)

  • 21. Localisation of cis regulatory elements at the beta-globin locus: analysis of hybrid haplotype chromosomes.
    Ofori-Acquah SF; Lalloz MR; Layton DM
    Biochem Biophys Res Commun; 1999 Jan; 254(1):181-7. PubMed ID: 9920754
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Identification of two novel beta zero-thalassemia mutations in a Filipino family: frameshift codon 67 (-TG) and a beta-globin gene deletion.
    Eng B; Chui DH; Saunderson J; Olivieri NF; Waye JS
    Hum Mutat; 1993; 2(5):375-9. PubMed ID: 8257991
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular spectrum of β-thalassemia mutations in the admixed Venezuelan population, and their linkage to β-globin gene haplotypes.
    Bravo-Urquiola M; Arends A; Gómez G; Montilla S; Gerard N; Chacin M; Berbar T; García O; García G; Velasquez D; Castillo O; Krishnamoorthy R
    Hemoglobin; 2012; 36(3):209-18. PubMed ID: 22563936
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN
    Hemoglobin; 2007; 31(2):233-41. PubMed ID: 17486506
    [TBL] [Abstract][Full Text] [Related]  

  • 26. HbA2-Partinico or delta(A2)Pro-->Thr, a new genetic variation in the delta-globin gene in cis to the beta(+) thal IVS-I-110 G>A, and the heterogeneity of delta-globin alleles in double heterozygotes for beta- and delta-globin gene defects.
    Lacerra G; Scarano C; Musollino G; Testa R; Prezioso R; Caruso DG; Lagona LF; Medulla E; Friscia MG; Gaudiano C; Carestia C
    Ann Hematol; 2010 Feb; 89(2):127-34. PubMed ID: 19609526
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
    Esteghamat F; Imanian H; Azarkeivan A; Pourfarzad F; Almadani N; Najmabadi H
    Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Beta-thalassemia intermedia due to two novel mutations in the promoter region of the beta-globin gene.
    Agouti I; Bennani M; Nezri M; Levy N; Badens C
    Eur J Haematol; 2008 Apr; 80(4):346-50. PubMed ID: 18081706
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [A rare transcription mutation (-90 C-->T) in a Chinese family with beta-thalassemia].
    Li WJ; Lao XW; Jai SQ; Liang FA; Mo QH; Ma JY; Xu XM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Dec; 20(6):468-70. PubMed ID: 14669211
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population.
    Colah R; Gorakshakar A; Nadkarni A; Phanasgaonkar S; Surve R; Sawant P; Mohanty D; Ghosh K
    Blood Cells Mol Dis; 2009; 42(3):241-6. PubMed ID: 19254853
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Most frequent beta-thalassemia mutations in the Argentinian population].
    Varela V; Abreu S; Rossetti LC; Targovnik H
    Sangre (Barc); 1996 Apr; 41(2):137-40. PubMed ID: 9045354
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Silent thalassemias: genotypes and phenotypes.
    Bianco I; Cappabianca MP; Foglietta E; Lerone M; Deidda G; Morlupi L; Grisanti P; Ponzini D; Rinaldi S; Graziani B
    Haematologica; 1997; 82(3):269-80. PubMed ID: 9234571
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular analysis of β-thalassemia patients: first identification of mutations HBB:c.93-2A>G and HBB:c.114G>A in Brazil.
    Fernandes AC; Shimmoto MM; Furuzawa GK; Vicari P; Figueiredo MS
    Hemoglobin; 2011; 35(4):358-66. PubMed ID: 21797703
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel Indian beta-thalassemia mutation in the CACCC box of the promoter region.
    Agarwal S; Arya V; Stolle CA; Pradhan M
    Eur J Haematol; 2006 Dec; 77(6):530-2. PubMed ID: 17042767
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Beta-globin cluster haplotypes in normal individuals and beta(0)39-thalassemia carriers from Sardinia, Italy.
    Piras I; Vona G; Falchi A; Latini V; Ristaldi S; Vacca L; Varesi L; Calò CM
    Am J Hum Biol; 2005; 17(6):765-72. PubMed ID: 16254903
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular heterogeneity of beta-thalassemia in Thailand.
    Fukumaki Y; Fucharoen S; Fucharoen G; Okamoto N; Ichinose M; Jetsrisuparb A; Sriroongrueng W; Nopparatana C; Laosombat V; Panich V
    Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():14-21. PubMed ID: 1363706
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular diagnosis of patients with beta-thalassemia major in central Taiwan by amplified created restriction site analysis.
    Peng CT; Wu JY; Tsai CH; Tsai FJ; Chang JG
    J Hum Genet; 1998; 43(4):237-41. PubMed ID: 9852674
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular characterization of beta-thalassemia in the Dohuk region of Iraq.
    Al-Allawi NA; Jubrael JM; Hughson M
    Hemoglobin; 2006; 30(4):479-86. PubMed ID: 16987803
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic heterogeneity of Beta thalassemia in Lebanon reflects historic and recent population migration.
    Makhoul NJ; Wells RS; Kaspar H; Shbaklo H; Taher A; Chakar N; Zalloua PA
    Ann Hum Genet; 2005 Jan; 69(Pt 1):55-66. PubMed ID: 15638828
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular spectrum of α- and β-globin gene mutations detected in the population of Guangxi Zhuang Autonomous Region, People's Republic of China.
    Zheng CG; Liu M; Du J; Chen K; Yang Y; Yang Z
    Hemoglobin; 2011; 35(1):28-39. PubMed ID: 21250879
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 47.