These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 1494543)

  • 41. [Detection of beta thalassemia by the technique of refractory amplification of mutation systems (ARMS-PCR)].
    Bravo M; Salazar R; Arends A; Alvarez M; Velázquez D; Guevara JM; Castillo O
    Invest Clin; 1999 Sep; 40(3):203-13. PubMed ID: 10531753
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Rapid, accurate genotyping of beta-thalassaemia mutations using a novel multiplex primer extension/denaturing high-performance liquid chromatography assay.
    Wu G; Hua L; Zhu J; Mo QH; Xu XM
    Br J Haematol; 2003 Jul; 122(2):311-6. PubMed ID: 12846902
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [Molecular analysis and prenatal diagnosis of beta-thalassemia: about our experience in central Tunisia].
    Laradi S; Haj Khelil A; Omri H; Chaieb A; Mahjoub T; Benlimam H; Amri F; Saad A; Miled A; Leturcq F; Ben Chibani J; Beldjord C
    Ann Biol Clin (Paris); 2000; 58(4):453-60. PubMed ID: 10932046
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Molecular genetics and prenatal diagnosis of beta thalassemia to control transfusion dependent births in carrier Pakistani couples.
    Kanwal S; Bukhari S; Perveen S
    J Pak Med Assoc; 2017 Jul; 67(7):1030-1034. PubMed ID: 28770881
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Molecular analysis of a thai beta-thalassaemia heterozygote with normal haemoglobin A2 level: implication for population screening.
    Fucharoen S; Fucharoen G; Sanchaisuriya K; Pengjam Y
    Ann Clin Biochem; 2002 Jan; 39(Pt 1):44-9. PubMed ID: 11853188
    [TBL] [Abstract][Full Text] [Related]  

  • 46. A beta-thalassaemia allele with 3 base substitution in codons 4/5 & 6 (ACT CCT GAG-> ACA TCT TAG) detected by denaturing gradient gel electrophoresis & sequencing.
    Saxena R; Moi L; Demurtas M; Rosatelli MC; Cao A; Verma IC
    Indian J Med Res; 2000 Jan; 111():24-7. PubMed ID: 10793490
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Filipino beta zero thalassaemia: a high Hb A2 beta zero thalassaemia resulting from a large deletion of the 5' beta globin gene region.
    Motum PI; Kearney A; Hamilton TJ; Trent RJ
    J Med Genet; 1993 Mar; 30(3):240-4. PubMed ID: 7682618
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [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]  

  • 49. [Accurate and rapid prenatal diagnosis of beta-thalassemia by a multiplex primer extension and denaturing high-performance liquid chromatography technique].
    Hua L; Zhu H; Li XR; Li J; Mo QH; Liao C; Hou YX; Zhong M; Xu XM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):600-3. PubMed ID: 15583991
    [TBL] [Abstract][Full Text] [Related]  

  • 50. The amplification refractory mutation system (ARMS): a rapid and direct prenatal diagnostic technique for beta-thalassaemia in Singapore.
    Tan JA; Tay JS; Lin LI; Kham SK; Chia JN; Chin TM; Aziz NB; Wong HB
    Prenat Diagn; 1994 Nov; 14(11):1077-82. PubMed ID: 7877957
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Molecular characterization of a novel 10.3 kb deletion causing beta-thalassaemia with unusually high Hb A2.
    Craig JE; Kelly SJ; Barnetson R; Thein SL
    Br J Haematol; 1992 Dec; 82(4):735-44. PubMed ID: 1482661
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Screening for mutations in human alpha-globin genes by nonradioactive single-strand conformation polymorphism.
    Jorge SB; Melo MB; Costa FF; Sonati MF
    Braz J Med Biol Res; 2003 Nov; 36(11):1471-4. PubMed ID: 14576901
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Accurate and rapid prenatal diagnosis of the most frequent East Mediterranean beta-thalassemia mutations.
    Naja RP; Kaspar H; Shbaklo H; Chakar N; Makhoul NJ; Zalloua PA
    Am J Hematol; 2004 Apr; 75(4):220-4. PubMed ID: 15054814
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Prenatal diagnosis for beta-thalassemia syndromes using HRP-labeled oligonucleotide probes at Siriraj Hospital.
    Winichagoon P; Fucharoen S; Siritanaratkul N; Tassana P; Thonglairoam V; Siriboon W; Kanokpongsakdi S
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():282-6. PubMed ID: 8629125
    [TBL] [Abstract][Full Text] [Related]  

  • 55. The risk of alpha-thalassaemia in offspring of beta-thalassaemia carriers in Hong Kong.
    Lam YH; Ghosh A; Tang MH; Chan V
    Prenat Diagn; 1997 Aug; 17(8):733-6. PubMed ID: 9267896
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Prenatal diagnosis of beta-thalassaemia: experience in a developing country.
    Saxena R; Jain PK; Thomas E; Verma IC
    Prenat Diagn; 1998 Jan; 18(1):1-7. PubMed ID: 9483634
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Efficiency and cost effectiveness: PAGE-SSCP versus MDE and Phast gels for the identification of unknown beta thalassaemia mutations.
    Gupta A; Agarwal S
    Mol Pathol; 2003 Aug; 56(4):237-9. PubMed ID: 12890746
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Analysis of beta-thalassemia mutations and prenated diagnosis in Chengdu population].
    Liu B; Fang J; Liu S; Ouyang X; Wang F; Liu L; Ma C; Huo P; Li Y
    Hua Xi Yi Ke Da Xue Xue Bao; 1995 Dec; 26(4):361-6. PubMed ID: 8732052
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Detection and molecular analysis of alpha and beta thalassaemia genes--recent developments in screening protocols.
    Tan J; Tay JS; Wong HB
    J Singapore Paediatr Soc; 1992; 34(1-2):53-6. PubMed ID: 1303468
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [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]  

    [Previous]   [Next]    [New Search]
    of 6.