382 related articles for article (PubMed ID: 18249014)
41. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
Darwish HM; El-Khatib FF; Ayesh S
Hemoglobin; 2005; 29(2):119-32. PubMed ID: 15921164
[TBL] [Abstract][Full Text] [Related]
42. Complexity of the alpha-globin genotypes identified with thalassemia screening in Sardinia.
Origa R; Paglietti ME; Sollaino MC; Desogus MF; Barella S; Loi D; Galanello R
Blood Cells Mol Dis; 2014 Jan; 52(1):46-9. PubMed ID: 23896219
[TBL] [Abstract][Full Text] [Related]
43. Co-inheritance of alpha and beta-thalassemia in a Jordanian family.
Al Qaddoumi AA
Clin Lab Sci; 2006; 19(3):165-8. PubMed ID: 16910233
[TBL] [Abstract][Full Text] [Related]
44. Detection of beta-thalassemia carrier by direct analysis of beta-globin gene lesions.
Pao CC; Lin CY; Tang GC; Sun CF; Hsieh TT
Biochem Biophys Res Commun; 1993 Mar; 191(3):1118-23. PubMed ID: 8466489
[TBL] [Abstract][Full Text] [Related]
45. Detection of unknown deletions in beta-globin gene cluster using relative quantitative PCR methods.
Babashah S; Jamali S; Mahdian R; Nosaeid MH; Karimipoor M; Alimohammadi R; Raeisi M; Maryami F; Masoudifar M; Zeinali S
Eur J Haematol; 2009 Sep; 83(3):261-9. PubMed ID: 19341428
[TBL] [Abstract][Full Text] [Related]
46. Nucleotide -88 (C-T) promoter mutation is a common beta-thalassemia mutation in the Jat Sikhs of Punjab, India.
Garewal G; Das R; Ahluwalia J; Marwaha RK; Varma S
Am J Hematol; 2005 Aug; 79(4):252-6. PubMed ID: 16044458
[TBL] [Abstract][Full Text] [Related]
47. Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH.
Blattner A; Brunner-Agten S; Ludin K; Hergersberg M; Herklotz R; Huber AR; Röthlisberger B
Blood Cells Mol Dis; 2013 Jun; 51(1):39-47. PubMed ID: 23491071
[TBL] [Abstract][Full Text] [Related]
48. Characterization of a novel deletion causing beta-thalassemia major in an Afghan family.
Gallienne AE; Iberson NM; Dréau HM; Jackson H; Bignell PA; Old JM; Schuh A; Henderson SJ
Hemoglobin; 2010; 34(1):110-4. PubMed ID: 20113295
[TBL] [Abstract][Full Text] [Related]
49. Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia.
Sollaino MC; Paglietti ME; Perseu L; Giagu N; Loi D; Galanello R
Haematologica; 2009 Oct; 94(10):1445-8. PubMed ID: 19794088
[TBL] [Abstract][Full Text] [Related]
50. Clinical phenotype of triplicated alpha-globin genes and heterozygosity for beta0-thalassemia in Chinese subjects.
Ma SK; Au WY; Chan AY; Chan LC
Int J Mol Med; 2001 Aug; 8(2):171-5. PubMed ID: 11445869
[TBL] [Abstract][Full Text] [Related]
51. [Association of alpha and beta thalassemia with alpha gene triplication in one family].
Villegas A; Muñoz JA; Risueño CF; Castro JM; Sánchez J; Ropero P; González FA
Med Clin (Barc); 1997 May; 108(20):781-3. PubMed ID: 9265084
[TBL] [Abstract][Full Text] [Related]
52. Different hematological phenotypes caused by the interaction of triplicated alpha-globin genes and heterozygous beta-thalassemia.
Camaschella C; Kattamis AC; Petroni D; Roetto A; Sivera P; Sbaiz L; Cohen A; Ohene-Frempong K; Trifillis P; Surrey S; Fortina P
Am J Hematol; 1997 Jun; 55(2):83-8. PubMed ID: 9209003
[TBL] [Abstract][Full Text] [Related]
53. Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia.
Rhodes SL; Plonczynski M; Harrell A; Li J; Safaya S; Files JC; Steinberg MH
Am J Med Sci; 1999 May; 317(5):341-5. PubMed ID: 10334122
[TBL] [Abstract][Full Text] [Related]
54. Molecular Basis of β-Thalassemia Intermedia in Erbil Province of Iraqi Kurdistan.
Shamoon RP; Al-Allawi NA; Cappellini MD; Di Pierro E; Brancaleoni V; Granata F
Hemoglobin; 2015; 39(3):178-83. PubMed ID: 25902180
[TBL] [Abstract][Full Text] [Related]
55. Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia.
Vinciguerra M; Passarello C; Cassarà F; Leto F; Cannata M; Calvaruso G; Di Maggio R; Renda D; Maggio A; Giambona A
Int J Lab Hematol; 2016 Feb; 38(1):17-26. PubMed ID: 26418075
[TBL] [Abstract][Full Text] [Related]
56. α-globin gene quadruplication and heterozygous β-thalassemia: a not so rare cause of thalassemia intermedia.
Origa R; Sollaino MC; Borgna-Pignatti C; Piga A; Feliu Torres A; Masile V; Galanello R
Acta Haematol; 2014; 131(3):162-4. PubMed ID: 24217654
[No Abstract] [Full Text] [Related]
57. Multiplex ligation-dependent probe amplification screening of isolated increased HbF levels revealed three cases of novel rearrangements/deletions in the beta-globin gene cluster.
Lee ST; Yoo EH; Kim JY; Kim JW; Ki CS
Br J Haematol; 2010 Jan; 148(1):154-60. PubMed ID: 19807730
[TBL] [Abstract][Full Text] [Related]
58. A stepwise α-thalassemia screening strategy in high-prevalence areas.
Alkindi SS; Alzadjali S; Daar S; Sindhuvi E; Wali Y; Pathare AV; Venugopal S; Lapoumeroulie C; Srivastava A; Krishnamoorthy R
Eur J Haematol; 2013 Aug; 91(2):164-9. PubMed ID: 23668236
[TBL] [Abstract][Full Text] [Related]
59. Combination of a triple alpha-globin gene with beta-thalassemia in a gypsy family: importance of the genetic testing in the diagnosis and search for a donor for bone marrow transplantation for one of their children.
Yus Cebrian F; Recasens Flores Mdel V; Izquierdo Álvarez S; Parra Salinas I; Rodriguez-Vigil Iturrate C
BMC Res Notes; 2016 Apr; 9():220. PubMed ID: 27080228
[TBL] [Abstract][Full Text] [Related]
60. Molecular mechanisms underlying thalassemia intermedia in Iran.
Neishabury M; Azarkeivan A; Oberkanins C; Esteghamat F; Amirizadeh N; Najmabadi H
Genet Test; 2008 Dec; 12(4):549-56. PubMed ID: 18939939
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]