140 related articles for article (PubMed ID: 16798641)
1. 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]
2. 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]
3. Beta-thalassemia due to a novel nonsense mutation at codon 37 (TGG-->TAG) found in an Afghanistani family.
Kornblit B; Taaning P; Birgens H
Hemoglobin; 2005; 29(3):209-13. PubMed ID: 16114184
[TBL] [Abstract][Full Text] [Related]
4. Nonsense β-thalassemia mutation at codon 37 (TGG>TGA), detected for the first time in three Turkish cases.
Bozdogan ST; Unsal C; Erkman H; Genc A; Yuregir OO; Muslumanoglu MH; Aslan H
Hemoglobin; 2012; 36(3):283-8. PubMed ID: 22385009
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Compound Heterozygosity for a Novel Mutation Codon 104 (-A) (
Qiu Y; Huang Y; Chen P; Wei S; Su Q; Zhang Z; Yang Z; Ye L; Huang J; Shen X; Mo W
Hemoglobin; 2020 Nov; 44(6):402-405. PubMed ID: 33198537
[TBL] [Abstract][Full Text] [Related]
8. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
Zhu BS; He J; Zhang J; Zeng XH; Su J; Xu XH; Li SY; Chen H; Zhang YH
Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis based on simultaneous DNA analysis for alpha- and beta-globin genes.
Oron-Karni V; Filon D; Rund D; Rachmilewitz E; Oppenheim A
Am J Hematol; 1996 Nov; 53(3):203-4. PubMed ID: 8895695
[No Abstract] [Full Text] [Related]
10. 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]
11. A β-Thalassemia Trait with Two Mutations in
Li J; Jiang F; Zhen L; Tang XW; Li DZ
Hemoglobin; 2019; 43(4-5):289-291. PubMed ID: 31690135
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Molecular defects in the beta-globin gene identified in different ethnic groups/populations during prenatal diagnosis for beta-thalassemia: a Malaysian experience.
Tan JA; George E; Tan KL; Chow T; Tan PC; Hassan J; Chia P; Subramanium R; Chandran R; Yap SF
Clin Exp Med; 2004 Dec; 4(3):142-7. PubMed ID: 15599663
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A wider molecular spectrum of beta-thalassaemia in Myanmar.
Win N; Harano T; Harano K; Myint TT; Mra R; Okada S; Shimono K; Myint AA
Br J Haematol; 2002 Jun; 117(4):988-92. PubMed ID: 12060142
[TBL] [Abstract][Full Text] [Related]
16. Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β
Li Y; Yan JM; Zhou JY; Lu YC; Li DZ
Hemoglobin; 2017 Jan; 41(1):47-49. PubMed ID: 28366026
[TBL] [Abstract][Full Text] [Related]
17. Direct genotyping and prenatal diagnosis of beta-thalassemia in Chinese by polymerase chain reaction mediated restriction fragment length polymorphism method.
Xu XM; Ma WF; Song LL; Xu Q; Zhang JZ
Clin Biochem; 1993 Dec; 26(6):497-503. PubMed ID: 7907284
[TBL] [Abstract][Full Text] [Related]
18. Detection of a rare beta-globin nonsense mutation [codon 59 (AAG-->TAG)] in an Italian family.
Amato A; Pia Cappabianca M; Ponzini D; Di Biagio P; Colosimo A; Guida V; Mastropietro F; Foglietta E; Grisanti P; Rinaldi S; Dallapiccola B; Bianco I
Hemoglobin; 2006; 30(3):405-7. PubMed ID: 16840234
[TBL] [Abstract][Full Text] [Related]
19. Beta-thalassemia mutations in the Portuguese; high frequencies of two alleles in restricted populations.
Tamagnini GP; Gonçalves P; Ribeiro ML; Kaeda J; Kutlar F; Baysal E; Huisman TH
Hemoglobin; 1993 Feb; 17(1):31-40. PubMed ID: 8454469
[TBL] [Abstract][Full Text] [Related]
20. Sistani population: a different spectrum of β-thalassemia mutations from other ethnic groups of Iran.
Miri-Moghaddam E; Zadeh-Vakili A; Nikravesh A; Sistani SS; Naroie-Nejad M
Hemoglobin; 2013; 37(2):138-47. PubMed ID: 23437895
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
