107 related articles for article (PubMed ID: 11939512)
1. A novel beta-thalassemia mutation in an Asian Indian.
Shaji RV; Gerard N; Krishnamoorthy R; Srivastava A; Chandy M
Hemoglobin; 2002 Feb; 26(1):49-57. PubMed ID: 11939512
[TBL] [Abstract][Full Text] [Related]
2. A novel 26 bp deletion [HBB: c.20_45del26bp] in exon 1 of the β-globin gene causing β-thalassemia major.
Edison ES; Venkatesan RS; Govindanattar SD; George B; Shaji RV
Hemoglobin; 2012; 36(1):98-102. PubMed ID: 22233277
[TBL] [Abstract][Full Text] [Related]
3. Coexistence of a novel beta-globin gene deletion (codons 81-87) with the codon 30 (G-->C) mutation in an Indian patient with beta0-thalassemia.
Shaji RV; Srivastava A; Krishnamoorthy R; Chandy M
Hemoglobin; 2002 Aug; 26(3):237-43. PubMed ID: 12403488
[TBL] [Abstract][Full Text] [Related]
4. Molecular mechanism of beta-thalassaemia caused by 22-bp duplication.
Svasti S; Boonchoy C; Vanichsetakul P; Winichagoon P; Fucharoen S
Ann Hematol; 2008 Aug; 87(8):633-7. PubMed ID: 18392622
[TBL] [Abstract][Full Text] [Related]
5. Molecular genetic testing of beta-thalassemia patients of Indian origin and a novel 8-bp deletion mutation at codons 36/37/38/39.
Gupta A; Hattori Y; Gupta UR; Sarwai S; Nigam N; Singhal P; Agarwal S
Genet Test; 2003; 7(2):163-8. PubMed ID: 12885342
[TBL] [Abstract][Full Text] [Related]
6. A novel beta0-thalassemia mutation at codon 55 (-A) and a rare 17 bp deletion at codons 126-131 in the Indian population.
Nadkarni A; Sakaguchi T; Takaku H; Gorakshakar A; Phanasgaonkar S; Colah RB; Mohanty D; Kiyama R
Hemoglobin; 2002 Feb; 26(1):41-7. PubMed ID: 11939511
[TBL] [Abstract][Full Text] [Related]
7. A 4 base pair TGAT insertion at codon 116 of the beta globin gene causes beta0-thalassemia.
Frischknecht H; Kiewitz R; Schmugge M
Haematologica; 2005 Nov; 90 Suppl():ECR20. PubMed ID: 16266911
[TBL] [Abstract][Full Text] [Related]
8. First report of a nonsense mutation at codon 15(TGG-->TAG) in exon 1 of the beta globin gene in a beta thalassemia trait in State of Orissa, India.
Nishank SS; Ranjit M; Chhotray GP
Hematology; 2008 Feb; 13(1):65-7. PubMed ID: 18534069
[TBL] [Abstract][Full Text] [Related]
9. Biallelic rare 17 bp deletion mutation (HBB:c.380_396 del TGCAGGCTGCCTATCAG) in a transfusion depended form of thalassemia.
Tripathi P; Agarwal S; Gupta A; Mandal K
Ann Hematol; 2020 Nov; 99(11):2719-2722. PubMed ID: 32296912
[No Abstract] [Full Text] [Related]
10. Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family.
He S; Lin L; Wei Y; Chen B; Yi S; Chen Q; Qiu X; Wei H; Li G; Zheng C
Hemoglobin; 2016 Aug; 40(4):277-9. PubMed ID: 27492766
[TBL] [Abstract][Full Text] [Related]
11. Identification of a novel frameshift mutation at codon 53 (-T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao family.
Yi P; Yu F; Huang S; Zhong C; Li Q; Yang Y; Zhang W; Xiao C; Xu X
Blood Cells Mol Dis; 2008; 41(1):56-9. PubMed ID: 18381244
[TBL] [Abstract][Full Text] [Related]
12. [New beta0-thalassaemic insertion mutation (CD 7/8, +G) in a Slovak family, associated with the Mediterranean haplotype IX].
Kynclová E; Divoký V; Kovaríková L; Melichárková R; Indráková J; Divoká M; Hammerová T; Sakalová A; Hudecek J; Indrák K
Vnitr Lek; 1999 Mar; 45(3):151-4. PubMed ID: 15641237
[TBL] [Abstract][Full Text] [Related]
13. Dominantly Inherited beta-Thalassemia.
Efremov GD
Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
[TBL] [Abstract][Full Text] [Related]
14. The novo 4 BP deletion in the codons 20/21 (-TGGA) at the first exon of the beta-globin gene causing a beta0-thalassemia in a Spanish male.
Ropero P; González FA; Villas JM; Paúl R; Villegas A
Ann Hematol; 2008 Jan; 87(1):63-5. PubMed ID: 17661037
[No Abstract] [Full Text] [Related]
15. 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]
16. A new β⁰-thalassemia frameshift mutation [β 48 (-T)] in a Uruguayan family.
Da Luz J; López P; Kimura EM; Albuquerque DM; Costa FF; Sans M; Sonati MF
Int J Lab Hematol; 2013 Feb; 35(1):111-4. PubMed ID: 22898041
[TBL] [Abstract][Full Text] [Related]
17. A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia.
Feriotto G; Salvatori F; Finotti A; Breveglieri G; Venturi M; Zuccato C; Bianchi N; Borgatti M; Lampronti I; Mancini I; Massei F; Favre C; Gambari R
Acta Haematol; 2008; 119(1):28-37. PubMed ID: 18230963
[TBL] [Abstract][Full Text] [Related]
18. Spectrum of beta-thalassemia mutations and their association with allelic sequence polymorphisms at the beta-globin gene cluster in an Eastern Indian population.
Kukreti R; Dash D; E VK; Chakravarty S; Das SK; De M; Talukder G
Am J Hematol; 2002 Aug; 70(4):269-77. PubMed ID: 12210807
[TBL] [Abstract][Full Text] [Related]
19. Nonsense codon mutations in the terminal exon of the beta-globin gene are not associated with a reduction in beta-mRNA accumulation: a mechanism for the phenotype of dominant beta-thalassemia.
Hall GW; Thein S
Blood; 1994 Apr; 83(8):2031-7. PubMed ID: 8161774
[TBL] [Abstract][Full Text] [Related]
20. A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia.
Jiang F; Huang LY; Chen GL; Zhou JY; Xie XM; Li DZ
Hemoglobin; 2017 Jan; 41(1):59-60. PubMed ID: 28460555
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]