154 related articles for article (PubMed ID: 18386005)
1. First detection of the codons 41-43 (-CTTTG,+A) beta-thalassemia mutation in a Chinese patient.
Liao C; Li DZ; Li J
Ann Hematol; 2008 Sep; 87(9):775-6. PubMed ID: 18386005
[No Abstract] [Full Text] [Related]
2. A novel beta-thalassemia mutation: frameshift at codon 59 detected in an Italian carrier.
Meloni A; Demurtas M; Moi L; Faà V; Cao A; Rosatelli MC
Hum Mutat; 1994; 3(3):309-11. PubMed ID: 8019567
[No Abstract] [Full Text] [Related]
3. First detection of the splice donor site IVS-I-2 (T-->B) beta-thalassemia mutation in a Chinese patient.
Liao C; Li J; Huang Y; Li D
Haematologica; 2005 Dec; 90(12):1695. PubMed ID: 16330445
[TBL] [Abstract][Full Text] [Related]
4. A double heterozygote for (deltabeta)0-thalassemia and codons 41/42 (-TTCT) behaves as a homozygote for the frameshift mutation in a Chinese family.
Liao C; Feng Q; Li J; Huang Y; Li D
Hemoglobin; 2007; 31(3):397-400. PubMed ID: 17654080
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Thalassemia beta0 due to an identical frameshift mutation, codon 15 (-T) in both parents.
Gajra B; Bandyopadhyay D; Chakrabarti S; Sengupta B; De M; Shaji RV; Talukder G
Am J Hematol; 2004 Feb; 75(2):117. PubMed ID: 14755384
[No Abstract] [Full Text] [Related]
7. Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.
Bibi A; Messaoud T; Fattoum S
Hemoglobin; 2006; 30(2):175-81. PubMed ID: 16798642
[TBL] [Abstract][Full Text] [Related]
8. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.
Li D; Liao C; Li J; Xie X; Huang Y; Zhong H
Haematologica; 2006 May; 91(5):649-51. PubMed ID: 16627247
[TBL] [Abstract][Full Text] [Related]
9. Japanese beta zero-thalassemia: molecular characterization of a novel insertion causing a stop codon.
Oshima K; Harano T; Harano K
Am J Hematol; 1996 May; 52(1):39-41. PubMed ID: 8638609
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A rare beta-thalassaemia mutation (C-T) at position -90 of the beta-globin gene discovered in a Chinese family.
Jia S; Lao X; Li W; Ma J; Mo Q; Xu X
Haematologica; 2003 Oct; 88(10):1191-3. PubMed ID: 14555318
[TBL] [Abstract][Full Text] [Related]
12. The codon 37 (TGG-->TAG) beta(0)-thalassemia mutation found in a Chinese family.
Li D; Liao C; Li J; Tang X
Hemoglobin; 2006; 30(2):171-3. PubMed ID: 16798641
[TBL] [Abstract][Full Text] [Related]
13. A new insertion mutation in the beta-globin gene [codons 45/46 (+A)] resulting in a beta-thalassemia minor phenotype.
Cornut G; Weng X; Robin L; Lavoie C; Marchand S; Soulières D
Hemoglobin; 2007; 31(3):393-5. PubMed ID: 17654079
[TBL] [Abstract][Full Text] [Related]
14. [Molecular characteristics of the thalassemia syndrome and prenatal diagnosis in a high risk family].
Vujić D; Cvorkov--Drazić M; Pavlović S; Bunjevacki G; Popović Z; Puzigaća Z
Srp Arh Celok Lek; 2001; 129 Suppl 1():56-8. PubMed ID: 15637993
[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. 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]
17. Another example of the beta-thalassemia mutation, IVS-I (-2) or codon 30 (A-->G), found in a Chinese family.
Li W; Hattori Y; Ohba Y; Okayama N; Lin WS; Long GF; Yamashiro Y; Yamamoto K; Yamamoto K
Hemoglobin; 1998 Jul; 22(4):377-81. PubMed ID: 9730368
[No Abstract] [Full Text] [Related]
18. Rare and unexpected mutations among Iranian beta-thalassemia patients and prenatal samples discovered by reverse-hybridization and DNA sequencing.
Najmabadi H; Pourfathollah AA; Neishabury M; Sahebjam F; Krugluger W; Oberkanins C
Haematologica; 2002 Oct; 87(10):1113-4. PubMed ID: 12368169
[No Abstract] [Full Text] [Related]
19. [Use of the polymerase chain reaction to detect beta-thalassemia mutations in heterozygous carriers from Azerbaijan while performing prenatal DNA-diagnosis].
Surin VL; Tagiev AF; Solov'ev GIa; Luk'ianenko AV; Plutalov OV; Berlin IuA
Genetika; 1993 May; 29(5):820-4. PubMed ID: 8335239
[TBL] [Abstract][Full Text] [Related]
20. Detection of two rare beta-thalassemia alleles found in the Tunisian population: codon 47 (+A) and codons 106/107 (+G).
Bibi A; Messaoud T; Beldjord C; Fattoum S
Hemoglobin; 2006; 30(4):437-47. PubMed ID: 16987798
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
