134 related articles for article (PubMed ID: 24725998)
1. The use of Taqman genotyping assays for rapid confirmation of β-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations.
Teh LK; Lee TY; Tan JA; Lai MI; George E
Int J Lab Hematol; 2015 Feb; 37(1):79-89. PubMed ID: 24725998
[TBL] [Abstract][Full Text] [Related]
2. The use of the amplification refractory mutation system (arms) in the detection of rare beta-thalassemia mutations in the Malays and Chinese in Malaysia.
Chan Yoke Fan ; Tan Kim Lian ; Wong Yean Ching ; Wee Yong Chui ; Yap Sook Fan ; Tan Jin Ai Mary Anne
Southeast Asian J Trop Med Public Health; 2001 Dec; 32(4):872-9. PubMed ID: 12041567
[TBL] [Abstract][Full Text] [Related]
3. Postnatal and non-invasive prenatal detection of β-thalassemia mutations based on Taqman genotyping assays.
Breveglieri G; Travan A; D'Aversa E; Cosenza LC; Pellegatti P; Guerra G; Gambari R; Borgatti M
PLoS One; 2017; 12(2):e0172756. PubMed ID: 28235086
[TBL] [Abstract][Full Text] [Related]
4. Detection of beta-globin gene mutations among Kelantan Malay thalassaemia patients by polymerase chain reaction restriction fragment length polymorphism.
Rozitah R; Nizam MZ; Nur Shafawati AR; Nor Atifah MA; Dewi M; Kannan TP; Ariffin N; Norsarwany M; Setianingsih I; Harahap A; Zilfalil BA
Singapore Med J; 2008 Dec; 49(12):1046-9. PubMed ID: 19122960
[TBL] [Abstract][Full Text] [Related]
5. Characterisation of beta-globin gene mutations in Malaysian children: a strategy for the control of beta-thalassaemia in a developing country.
Thong MK; Tan JA; Tan KL; Yap SF
J Trop Pediatr; 2005 Dec; 51(6):328-33. PubMed ID: 15967770
[TBL] [Abstract][Full Text] [Related]
6. Genotyping of β-globin gene mutations in single lymphocytes: a preliminary study for preimplantation genetic diagnosis of monogenic disorders.
Durmaz B; Ozkinay F; Onay H; Karaca E; Aydinok Y; Tavmergen E; Vrettou C; Traeger-Synodinos J; Kanavakis E
Hemoglobin; 2012; 36(3):230-43. PubMed ID: 22524255
[TBL] [Abstract][Full Text] [Related]
7. Specific and straightforward molecular investigation of β-thalassemia mutations in the Malaysian Malays and Chinese using direct TaqMan genotyping assays.
Kho SL; Chua KH; George E; Tan JA
Genet Mol Res; 2013 Jul; 12(3):2409-15. PubMed ID: 23479149
[TBL] [Abstract][Full Text] [Related]
8. Investigation of sensitivity, specificity and accuracy of Tetra primer ARMS PCR method in comparison with conventional ARMS PCR, based on sequencing technique outcomes in IVS-II-I genotyping of beta thalassemia patients.
Honardoost MA; Tabatabaeian H; Akbari M; Salehi M
Gene; 2014 Oct; 549(1):1-6. PubMed ID: 24946023
[TBL] [Abstract][Full Text] [Related]
9. Detection of β-Thalassemia Mutations Using TaqMan Single Nucleotide Polymorphism Genotyping Assays.
Alwazani WA; Zahid R; Elaimi A; Bajouh O; Hindawi S; Arab B; Damanhouri G; Saka MY; Turki R; Khan JA; Dallol A; Abuzenadah AM
Genet Test Mol Biomarkers; 2016 Mar; 20(3):154-7. PubMed ID: 26890443
[TBL] [Abstract][Full Text] [Related]
10. Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian population.
Italia K; Sawant P; Surve R; Wadia M; Nadkarni A; Ghosh K; Colah R
Eur J Haematol; 2012 Aug; 89(2):160-4. PubMed ID: 22690826
[TBL] [Abstract][Full Text] [Related]
11. Spectrum of beta-thalassaemia mutations in transfusion dependent thalassaemia patients: practical implications in prenatal diagnosis.
George E; George R; Ariffin WA; Mokhtar AB; Azman ZA; Sivagengei K
Med J Malaysia; 1993 Sep; 48(3):325-9. PubMed ID: 8183146
[TBL] [Abstract][Full Text] [Related]
12. High throughput molecular confirmation of β-thalassemia mutations using novel TaqMan probes.
Kho SL; Chua KH; George E; Tan JA
Sensors (Basel); 2013 Feb; 13(2):2506-14. PubMed ID: 23429513
[TBL] [Abstract][Full Text] [Related]
13. A new genotyping method for detecting low abundance single nucleotide mutations based on gap ligase chain reaction and quantitative PCR assay.
Yi P; Jiang H; Li L; Dai F; Zheng Y; Han J; Chen Z; Guo J
Cell Biochem Biophys; 2012 Jan; 62(1):161-7. PubMed ID: 22006255
[TBL] [Abstract][Full Text] [Related]
14. Molecular characterization of α- and β-thalassaemia among Malay patients.
Yatim NF; Rahim MA; Menon K; Al-Hassan FM; Ahmad R; Manocha AB; Saleem M; Yahaya BH
Int J Mol Sci; 2014 May; 15(5):8835-45. PubMed ID: 24857915
[TBL] [Abstract][Full Text] [Related]
15. A multiplex ARMS PCR approach to detection of common β-globin gene mutations.
Mishra KK; Patel P; Bhukhanvala DS; Shah A; Ghosh K
Anal Biochem; 2017 Nov; 537():93-98. PubMed ID: 28669707
[TBL] [Abstract][Full Text] [Related]
16. Non-invasive prenatal diagnosis using fetal DNA in maternal plasma: a preliminary study for identification of paternally-inherited alleles using single nucleotide polymorphisms.
Chen JJ; Tan JA; Chua KH; Tan PC; George E
BMJ Open; 2015 Jul; 5(7):e007648. PubMed ID: 26201722
[TBL] [Abstract][Full Text] [Related]
17. Reverse dot-blot detection of Thai beta-thalassaemia mutations.
Sutcharitchan P; Saiki R; Fucharoen S; Winichagoon P; Erlich H; Embury SH
Br J Haematol; 1995 Aug; 90(4):809-16. PubMed ID: 7669658
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of beta-thalassaemia mutations using the reverse dot blot technique.
Muralitharan S; Srivastava A; Shaji RV; Mathai M; Srivastava VM; Dennison D; Lu CY; Krishnamoorthy R
Natl Med J India; 1996; 9(2):70-1. PubMed ID: 8857041
[TBL] [Abstract][Full Text] [Related]
19. ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia.
Shammas C; Papasavva T; Felekis X; Christophorou C; Roomere H; Synodinos JT; Kanavakis E; El-Khateeb M; Hamamy H; Mahmoud T; Shboul M; El Beshlawy A; Filon D; Hussein IR; Galanello R; Romeo G; Kleanthous M
Clin Chem Lab Med; 2010 Dec; 48(12):1713-8. PubMed ID: 20704537
[TBL] [Abstract][Full Text] [Related]
20. Evaluation of the BeTha gene 1 kit for the qualitative detection of the eight most common Mediterranean beta-thalassemia mutations.
Ugozzoli LA; Lowery JD; Reyes AA; Lin CI; Re A; Locati F; Galanello R; Macioni L; Maggio A; Giambona A; Loutradi A; Boussiou M; Wallace RB
Am J Hematol; 1998 Nov; 59(3):214-22. PubMed ID: 9798659
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]