116 related articles for article (PubMed ID: 11939511)
1. 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]
2. 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]
3. Two new beta0-thalassemic mutations: a deletion (-CC) at codon 142 or overlapping codons 142-143, and an insertion (+T) at codon 45 or overlapping codons 44-45/45-46 of the beta-globin gene.
Lacan P; Aubry M; Couprie N; Francina A
Hemoglobin; 2007; 31(2):159-65. PubMed ID: 17486497
[TBL] [Abstract][Full Text] [Related]
4. Molecular pathogenesis and clinical variability of homozygous beta0-thalassemia in populations of Jammu region of J&K state (India).
Singh SP; Gupta S
Hematology; 2006 Aug; 11(4):271-5. PubMed ID: 17178667
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Molecular genetic analyses of beta-thalassemia in South India reveals rare mutations in the beta-globin gene.
Bashyam MD; Bashyam L; Savithri GR; Gopikrishna M; Sangal V; Devi ARR
J Hum Genet; 2004; 49(8):408-413. PubMed ID: 15278762
[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. Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
Colah R; Nadkarni A; Gorakshakar A; Phanasgaonkar S; Surve R; Subramaniam PG; Bondge N; Pujari K; Ghosh K; Mohanty D
Blood Cells Mol Dis; 2004; 33(2):153-7. PubMed ID: 15315795
[TBL] [Abstract][Full Text] [Related]
9. Beta-thalassemia in the Korean population.
Park SS; Lee YJ; Kim JY; Joo SI; Hattori Y; Ohba Y; Cho HI
Hemoglobin; 2002 May; 26(2):135-45. PubMed ID: 12144056
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A novel deletion in a Turkish beta-thalassemia patient detected by DGGE and direct sequencing: FSC 22-24 (-7 bp).
Ozçelik H; Başak AN; Tüzmen S; Kirdar B; Akar N
Hemoglobin; 1993 Aug; 17(4):387-91. PubMed ID: 8226099
[No Abstract] [Full Text] [Related]
12. 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]
13. The spectrum of beta-thalassemia mutations in southern Thailand.
Nopparatana C; Panich V; Saechan V; Sriroongrueng V; Nopparatana C; Rungjeadpha J; Pornpatkul M; Laosombat V; Fukumaki Y
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():229-34. PubMed ID: 8629112
[TBL] [Abstract][Full Text] [Related]
14. Molecular basis of beta-thalassemia in the Maldives.
Furuumi H; Firdous N; Inoue T; Ohta H; Winichagoon P; Fucharoen S; Fukumaki Y
Hemoglobin; 1998 Mar; 22(2):141-51. PubMed ID: 9576331
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Prenatal diagnosis of beta-thalassemia major by high-performance liquid chromatography analysis of hemoglobins in fetal blood samples.
Sanguansermsri T; Thanarattanakorn P; Steger HF; Tongsong T; Chanprapaph P; Wanpirak C; Siriwatanapa P; Sirichotiyakul S; Flatz G
Hemoglobin; 2001 Feb; 25(1):19-27. PubMed ID: 11300346
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. A new frameshift mutation, insertion of ATCT, at codon 48 in the beta-globin gene causes beta-thalassemia in an Indian proband.
Jain PK; Dozy AM; Verma IC; Chehab FF
Hum Mutat; 1994; 3(4):397-8. PubMed ID: 8081396
[No Abstract] [Full Text] [Related]
20. [Molecular nature of beta-thalassemia in Tajikistan: a four base pair deletion in codons 41-42 of the beta-globin gene].
Kolesnikova TN; Surin VL; Moliaka IuK; Luk'ianenko AV; Tagiev AF; Asanov AIu; Bobokhodzhaev ZM; Solov'ev GIa
Genetika; 1992 Nov; 28(11):28-33. PubMed ID: 1286798
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
