123 related articles for article (PubMed ID: 16189162)
21. Dominant β-thalassaemia with unusually high Hb A
Singha K; Karnpean R; Fucharoen G; Fucharoen S
J Clin Pathol; 2020 Aug; 73(8):511-513. PubMed ID: 31879269
[TBL] [Abstract][Full Text] [Related]
22. A deletion of 11 bp (CD 131-134) in exon 3 of the beta-globin gene produces the phenotype of inclusion body beta-thalassemia.
Ropero P; Villegas A; Martínez M; Ataulfo González Fernández F; Benavente C; Mateo M
Ann Hematol; 2005 Sep; 84(9):584-7. PubMed ID: 15977037
[TBL] [Abstract][Full Text] [Related]
23. A novel beta-thalassaemia mutation in the 5' untranslated region of the beta-globin gene.
Athanassiadou A; Papachatzopoulou A; Zoumbos N; Maniatis GM; Gibbs R
Br J Haematol; 1994 Oct; 88(2):307-10. PubMed ID: 7803275
[TBL] [Abstract][Full Text] [Related]
24. Silent carrier beta-thalassaemia due to a severe beta-globin mutation interacting with other genetic elements.
Rund D; Filon D; Oppenheim A; Abramov A
Eur J Pediatr; 1993 Jul; 152(7):574-6. PubMed ID: 8354316
[TBL] [Abstract][Full Text] [Related]
25. Haematological phenotypes in a family with triplicated alpha-globin gene, beta zero 39 and delta+27 thalassaemia mutations.
Oggiano L; Rimini E; Frogheri L; Guiso L; Pistidda P; Longinotti M
Clin Lab Haematol; 1992; 14(4):289-92. PubMed ID: 1478008
[TBL] [Abstract][Full Text] [Related]
26. A beta zero-thalassaemia due to a 1605 bp deletion of the 5' beta-globin gene region.
Dimovski AJ; Efremov DG; Jankovic L; Plaseska D; Juricic D; Efremov GD
Br J Haematol; 1993 Sep; 85(1):143-7. PubMed ID: 8251381
[TBL] [Abstract][Full Text] [Related]
27. Beta-thalassemia unlinked to the beta-globin gene in an English family.
Thein SL; Wood WG; Wickramasinghe SN; Galvin MC
Blood; 1993 Aug; 82(3):961-7. PubMed ID: 8101733
[TBL] [Abstract][Full Text] [Related]
28. [Molecular diagnosis in a Korean family with thalassemia intermedia due to co-inheritance of triplicated alpha-globin genes (alphaalpha/alphaalphaalpha(anti 3.7)) and beta-thalassemia trait (IVS-II-1 G-->A)].
Chen M; Han JY; Sun Q; Kim IH; Ren Z; Huang S; Zeng Y
Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):195-7. PubMed ID: 11876981
[TBL] [Abstract][Full Text] [Related]
29. Severe thalassaemia intermedia caused by interaction of homozygosity for alpha-globin gene triplication with heterozygosity for beta zero-thalassaemia.
Oron V; Filon D; Oppenheim A; Rund D
Br J Haematol; 1994 Feb; 86(2):377-9. PubMed ID: 8199028
[TBL] [Abstract][Full Text] [Related]
30. A novel beta-globin structural mutant, Hb Brescia (beta 114 Leu-Pro), causing a severe beta-thalassemia intermedia phenotype.
Murru S; Poddie D; Sciarratta GV; Agosti S; Baffico M; Melevendi C; Pirastu M; Cao A
Hum Mutat; 1992; 1(2):124-8. PubMed ID: 1301199
[TBL] [Abstract][Full Text] [Related]
31. New frameshift mutation, insertion of A, at codon 95 of the beta-globin gene causes beta-thalassemia in two Vietnamese families.
Cai S; Chehab FF
Hum Mutat; 1996; 8(3):293-4. PubMed ID: 8889595
[No Abstract] [Full Text] [Related]
32. 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]
33. Hb Wilde and Hb Patagonia: two novel elongated beta-globin variants causing dominant beta-thalassemia.
Scheps KG; Hasenahuer MA; Parisi G; Fornasari MS; Pennesi SP; Erramouspe B; Basack FN; Veber ES; Aversa L; Elena G; Varela V
Eur J Haematol; 2015 Jun; 94(6):498-503. PubMed ID: 25284604
[TBL] [Abstract][Full Text] [Related]
34. Initiation codon mutation (ATG --> ATA) of the beta-globin gene causing beta-thalassemia in a Swedish family.
Landin B; Rudolphi O; Ek B
Am J Hematol; 1995 Mar; 48(3):158-62. PubMed ID: 7864023
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Three new beta-thalassemia mutations with varying degrees of severity.
Frischknecht H; Dutly F; Walker L; Nakamura-Garrett LM; Eng B; Waye JS
Hemoglobin; 2009; 33(3):220-5. PubMed ID: 19657836
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. [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]
39. 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]
40. Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.
Galanello R; Perseu L; Perra C; Maccioni L; Barella S; Longinotti M; Cao A; Cazzola M
Br J Haematol; 2004 Dec; 127(5):604-6. PubMed ID: 15566365
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
