BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

466 related articles for article (PubMed ID: 19609526)

  • 21. Haplotype analysis of beta thalassemia patients in Western Iran.
    Rahimi Z; Muniz A; Akramipour R; Tofieghzadeh F; Mozafari H; Vaisi-Raygani A; Parsian A
    Blood Cells Mol Dis; 2009; 42(2):140-3. PubMed ID: 19141369
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Masking of a β-thalassemia determinant by a novel δ-globin gene defect [Hb A2-Saurashtra or δ100(G2)Pro→Ser; HBD: c.301C>T] in Cis.
    Colaco S; Trivedi A; Colah RB; Ghosh K; Nadkarni AH
    Hemoglobin; 2014; 38(1):24-7. PubMed ID: 24200152
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification of a novel δ-globin gene mutation in an Iranian family.
    Amirian A; Jafarinejad M; Kordafshari AR; Mosayyebzadeh M; Karimipoor M; Zeinali S
    Hemoglobin; 2010; 34(6):594-8. PubMed ID: 21077769
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Known and new delta globin gene mutations and their diagnostic significance.
    Bouva MJ; Harteveld CL; van Delft P; Giordano PC
    Haematologica; 2006 Jan; 91(1):129-32. PubMed ID: 16434382
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Phenotypes of individuals with a beta thal classical allele associated either with a beta thal silent allele or with alpha globin gene triplication.
    Bianco I; Lerone M; Foglietta E; Deidda G; Cappabianca MP; Morlupi L; Ponzini D; Grisanti P; Di Biagio P; Amato A; Mezzabotta M; Graziani B
    Haematologica; 1997; 82(5):513-25. PubMed ID: 9407714
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Characterization of three novel delta chain hemoglobin variants and two delta-thalassemia alleles.
    Frischknecht H; Troxler H; Dutly F; Walker L; Hohenadel BA; Eng B; Waye JS
    Hemoglobin; 2010; 34(4):374-82. PubMed ID: 20642335
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Normal Hb A2 β-thalassemia trait: frameshift mutation (HBB: c.187_251dup) in cis with the Hb A2' δ-globin gene missense mutation (HBD: c.49G>C).
    Waye JS; Eng B; Hellens L; Hohenadel BA; Nakamura LM; Walker L
    Hemoglobin; 2013; 37(2):201-4. PubMed ID: 23398055
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family.
    Galanello R; Podda A; Melis MA; Monne M; Cao A
    Prog Clin Biol Res; 1989; 316B():113-21. PubMed ID: 2482492
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Spectrum of beta thalassemia mutations and HbF levels in the heterozygous Moroccan population.
    Lemsaddek W; Picanço I; Seuanes F; Mahmal L; Benchekroun S; Khattab M; Nogueira P; Osório-Almeida L
    Am J Hematol; 2003 Jul; 73(3):161-8. PubMed ID: 12827652
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patients.
    Harteveld CL; Refaldi C; Cassinerio E; Cappellini MD; Giordano PC
    Blood Cells Mol Dis; 2008; 40(3):312-6. PubMed ID: 18249014
    [TBL] [Abstract][Full Text] [Related]  

  • 31. New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG].
    Phylipsen M; Harteveld CL; de Metz M; Gallivan MV; Arkesteijn SG; Luo HY; Chui DH; Giordano PC
    Hemoglobin; 2010; 34(5):445-50. PubMed ID: 20854118
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicine.
    Akerman BR; Fujiwara TM; Lancaster GA; Morgan K; Scriver CR
    Am J Med Genet; 1990 May; 36(1):76-84. PubMed ID: 2333910
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Association in cis of the mutations +20 (C>T) in the 5' untranslated region and IVS-II-745 (C>G) on the β-globin gene.
    Ropero P; González FA; Cela E; Beléndez C; Cervera A; Martínez-Nieto J; de la Fuente-Gonzalo F; Vinuesa L; Villegas A; Díaz-Mediavilla J
    Hemoglobin; 2013; 37(2):112-8. PubMed ID: 23425204
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Henderson SJ; Timbs AT; McCarthy J; Gallienne AE; Proven M; Rugless MJ; Lopez H; Eglinton J; Dziedzic D; Beardsall M; Khalil MS; Old JM
    Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
    Moassas F; Nweder MS; Murad H
    BMC Pediatr; 2019 Feb; 19(1):61. PubMed ID: 30777047
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Dominantly Inherited beta-Thalassemia.
    Efremov GD
    Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Two novel mutations in the 3' untranslated region of the beta-globin gene that are associated with the mild phenotype of beta thalassemia.
    Bilgen T; Clark OA; Ozturk Z; Akif Yesilipek M; Keser I
    Int J Lab Hematol; 2013 Feb; 35(1):26-30. PubMed ID: 22862814
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Two new delta-globin mutations: Hb A2-Ninive [delta133(H11)Val-Ala] and a delta(+)-thalassemia mutation [-31 (A --> G)] in the TATA box of the delta-globin gene.
    Frischknecht H; Dutly F
    Hemoglobin; 2005; 29(2):151-4. PubMed ID: 15921167
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of the linkage of a 1.357 KB beta-globin gene deletion and A gamma-globin gene triplication in a Chinese family.
    Lou JW; Li Q; Wei XF; Huang JW; Xu XM
    Hemoglobin; 2010; 34(4):343-53. PubMed ID: 20642332
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Characterization of the 5' and 3' breakpoints of the Spanish (δβ)0-thalassemia deletion in Mexican patients.
    Guzmán LF; Perea FJ; Morales-González KR; Sánchez-López JY; de la Cruz EI; Chávez-Velasco ML; Ibarra CB
    Hemoglobin; 2011; 35(1):80-3. PubMed ID: 21250884
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 24.