211 related articles for article (PubMed ID: 20642332)
1. 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]
2. Molecular characterization of a beta-globin gene deletion of 1357 bp in a Taiwanese beta-thalassemia carrier.
Huang CH; Chang YY; Chen CH; Ko TM
Hemoglobin; 2008; 32(5):498-504. PubMed ID: 18932076
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. The carrier frequency of α-globin gene triplication in an Iranian population with normal or borderline hematological parameters.
Moosavi SF; Amirian A; Zarbakhsh B; Kordafshari A; Mirzahoseini H; Zeinali S; Karimipoor M
Hemoglobin; 2011; 35(4):323-30. PubMed ID: 21797699
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Identification and molecular characterization of a novel 55-kb deletion recurrent in southern Italy: the Italian (G) γ((A) γδβ)°-thalassemia.
Lacerra G; Prezioso R; Musollino G; Piluso G; Mastrullo L; De Angioletti M
Eur J Haematol; 2013 Mar; 90(3):214-9. PubMed ID: 23281611
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Molecular characterization of a novel 55.1 kb (G)gamma((A)gammadeltabeta)(0)-thalassemia deletion in two Canadian families.
Voruganti I; Eng B; Waye JS
Hemoglobin; 2009; 33(6):422-7. PubMed ID: 19958187
[TBL] [Abstract][Full Text] [Related]
9. [Beta-thalassemia mutations and single nucleotide polymorphism at -158 of Ggamma-globin gene associated with altered levels of Hb F in beta-thalassemia heterozygotes].
Chen JF; Long GF; Lin WX; Chen P
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):498-501. PubMed ID: 15476181
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Molecular characterization of a Chinese pedigree with beta-thalassemia intermedia.
Huang G; Jiang WL; Rong KB; Li YX; Luo XL; Meng JX; Yu XY
Hemoglobin; 2010 Jan; 34(2):179-83. PubMed ID: 20353356
[TBL] [Abstract][Full Text] [Related]
12. A Family with γ-Thalassemia and High Hb A2 Levels.
Parmeggiani G; Gualandi F; Selvatici R; Rimessi P; Bigoni S; Taddei Masieri M; Dolcini B; Venturoli A; Cappabianca MP; Ferlini A; Ravani A
Hemoglobin; 2016 Jun; 40(3):187-90. PubMed ID: 27117568
[TBL] [Abstract][Full Text] [Related]
13. Mutational spectrum of delta-globin gene in the Portuguese population.
Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients.
Fucharoen S; Pengjam Y; Surapot S; Fucharoen G; Sanchaisuriya K
Am J Hematol; 2002 Oct; 71(2):109-13. PubMed ID: 12353310
[TBL] [Abstract][Full Text] [Related]
20. [Molecular diagnosis of beta-thalassemia intermedia].
Chen J; Liu W; Chen M
Zhonghua Yi Xue Za Zhi; 1997 Aug; 77(8):575-8. PubMed ID: 9772460
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
