276 related articles for article (PubMed ID: 2139713)
1. [Testing of G----A mutation in position 110 of a minor intron of beta-globin genes in patients with thalassemia in Azerbaijan].
Fedorov AN; Rasulov EM; Oretskaia TS; Lebedeva IV; Ivanovskaia MG; Shabarova ZA; Limborskaia SA
Mol Gen Mikrobiol Virusol; 1990 Jan; (1):18-22. PubMed ID: 2139713
[TBL] [Abstract][Full Text] [Related]
2. [Molecular causes of thalassemia. IV. Cloning of the beta-globin gene in a patient with beta-thalassemia from Azerbaijan and determination of the point mutation in a minor intron].
Limborskaia SA; Bukhman VL; Prosniak MI; Fedorov AN; Slominskiĭ PA
Genetika; 1987 Feb; 23(2):228-38. PubMed ID: 3030889
[TBL] [Abstract][Full Text] [Related]
3. A new mutation in the beta-globin gene (IVS II-850 G-C) found in a Yugoslavian beta-thalassemia heterozygote.
Jankovic L; Dimovski AJ; Sukarova E; Juricic D; Efremov GD
Haematologica; 1992; 77(2):119-21. PubMed ID: 1398296
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Molecular genetics of the thalassemias in Argentina].
Varela V; Rossetti LC; Binaghi A; Targovnik HM; Abreu MS
Sangre (Barc); 1999 Jun; 44(3):210-5. PubMed ID: 10481583
[TBL] [Abstract][Full Text] [Related]
6. [A novel Chinese beta-thalassemia mutation--4bp deletion (AAAC) downstream from the cap site].
Xu Y
Zhonghua Yi Xue Za Zhi; 1991 Apr; 71(4):205-7, 16. PubMed ID: 1650632
[TBL] [Abstract][Full Text] [Related]
7. [New single point mutation at the initiation codon (ATG-AGG) identified in amplified genomic DNA of a Chinese with beta-thalassaemia].
Xie S
Zhonghua Yi Xue Za Zhi; 1990 May; 70(5):258-61, 20. PubMed ID: 1975769
[TBL] [Abstract][Full Text] [Related]
8. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
El-Gawhary S; El-Shafie S; Niazi M; Aziz M; El-Beshlawy A
Hemoglobin; 2007; 31(1):63-9. PubMed ID: 17365006
[TBL] [Abstract][Full Text] [Related]
9. [Analysis of RFLP haplotypes in the beta-globin gene cluster and the identification of beta-thalassemia genes in patients from Guangdong Province].
Li J
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1992 Feb; 14(1):42-5. PubMed ID: 1350518
[TBL] [Abstract][Full Text] [Related]
10. Characterization of beta-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA.
Wong C; Dowling CE; Saiki RK; Higuchi RG; Erlich HA; Kazazian HH
Nature; 1987 Nov 26-Dec 2; 330(6146):384-6. PubMed ID: 3683554
[TBL] [Abstract][Full Text] [Related]
11. [Character of two mutations of the beta-globin gene in beta 0-thalassemia in Azerbaijan].
Gol'tsov AA; Surin VL; Luk'ianenko AV; Alekseev AA; Kaboev OK; Vinogradov SV; Solov'ev GIa; Berlin IuA; Shvarts EI
Bioorg Khim; 1989 Jul; 15(7):1001-2. PubMed ID: 2530988
[TBL] [Abstract][Full Text] [Related]
12. Analysis of beta-thalassemia mutations and beta-locus control region hypersensitive sites 2, 3 and 4 in southern Thailand.
Sriroongrueng W; Schleiemacher E; Panich V; Nopparatana C; Saechan V; Laosombat V; Pornpatkul M; Fukumaki Y
Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():120-7. PubMed ID: 9640613
[TBL] [Abstract][Full Text] [Related]
13. [Molecular causes of thalassemia. III. Molecular genetic variants of beta-thalassemia in Azerbaijan].
Dergunova LV; Slominskiĭ PA; Rustamov RSh; Dadasheva TS; Amzashvili MG
Genetika; 1982 Jul; 18(7):1045-55. PubMed ID: 6180957
[TBL] [Abstract][Full Text] [Related]
14. Molecular pathology and detection of beta-thalassemias.
Cao A; Murru S
Prog Clin Biol Res; 1989; 309():3-11. PubMed ID: 2675099
[TBL] [Abstract][Full Text] [Related]
15. A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosis.
Fucharoen S; Fucharoen G; Ratanasiri T; Jetsrisuparb A; Fukumaki Y
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():278-81. PubMed ID: 8629124
[TBL] [Abstract][Full Text] [Related]
16. Molecular diagnosis of A gamma hereditary persistence of fetal hemoglobin using polymerase chain reaction and oligonucleotide analysis.
Gottardi E; Alfarano A; Serra A; Sciarratta G; Bertero MT; Saglio G; Camaschella C
Haematologica; 1990; 75(1):17-20. PubMed ID: 1692560
[TBL] [Abstract][Full Text] [Related]
17. [Most frequent beta-thalassemia mutations in the Argentinian population].
Varela V; Abreu S; Rossetti LC; Targovnik H
Sangre (Barc); 1996 Apr; 41(2):137-40. PubMed ID: 9045354
[TBL] [Abstract][Full Text] [Related]
18. Heterogeneity of beta-thalassemia in Azerbaidzhan.
Dergunova LV; Ryskov AP; Slominsky PA; Rustamov RS; Limborska SA
Haematologia (Budap); 1984; 17(4):473-81. PubMed ID: 6241915
[TBL] [Abstract][Full Text] [Related]
19. "Silent" nucleotide substitution in codon 24 of a beta+ thalassemia globin gene activates splice site in coding sequence RNA.
Humphries RK; Ley T; Goldsmith ME; Kantor JA; Cline AC; Nienhuis AW
Prog Clin Biol Res; 1983; 134():123-6. PubMed ID: 6664994
[TBL] [Abstract][Full Text] [Related]
20. Silent thalassemias: genotypes and phenotypes.
Bianco I; Cappabianca MP; Foglietta E; Lerone M; Deidda G; Morlupi L; Grisanti P; Ponzini D; Rinaldi S; Graziani B
Haematologica; 1997; 82(3):269-80. PubMed ID: 9234571
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]