123 related articles for article (PubMed ID: 35701141)
1. One-step genotyping of α-thalassaemia by multiplex symmetric PCR melting curve.
Qin J; He J; Li Y; Liu N; Tao F; Zhang P; Guo W; Qin Q; Zhou W
J Clin Pathol; 2023 Sep; 76(9):632-636. PubMed ID: 35701141
[TBL] [Abstract][Full Text] [Related]
2. Screening for clinically significant non-deletional alpha thalassaemia mutations by pyrosequencing.
Haywood A; Dreau H; Timbs A; Schuh A; Old J; Henderson S
Ann Hematol; 2010 Dec; 89(12):1215-21. PubMed ID: 20567827
[TBL] [Abstract][Full Text] [Related]
3. A Nested Asymmetric PCR Melting Curve Assay for One-Step Genotyping of Nondeletional α-Thalassemia Mutations.
Qin J; Xu M; Zhang Q; Wen X; He S; Zhou Y; Liu H; Zhou W
J Mol Diagn; 2020 Jun; 22(6):794-800. PubMed ID: 32482310
[TBL] [Abstract][Full Text] [Related]
4. A laboratory strategy for genotyping haemoglobin H disease in the Chinese.
Chan AY; So CC; Ma ES; Chan LC
J Clin Pathol; 2007 Aug; 60(8):931-4. PubMed ID: 17018682
[TBL] [Abstract][Full Text] [Related]
5. Simultaneous Genotyping of α-Thalassemia Deletional and Nondeletional Mutations by Real-Time PCR-Based Multicolor Melting Curve Analysis.
Huang Q; Wang X; Tang N; Yan T; Chen P; Li Q
J Mol Diagn; 2017 Jul; 19(4):567-574. PubMed ID: 28506685
[TBL] [Abstract][Full Text] [Related]
6. Simultaneous Characterization of Deletional and Nondeletional Globin Gene Mutations by Multiplex Real-Time-Polymerase Chain Reaction and High-Resolution Melting Curve Analysis.
Nuinoon M; Horpet D
Hemoglobin; 2020 Sep; 44(5):311-318. PubMed ID: 32783482
[TBL] [Abstract][Full Text] [Related]
7. A comprehensive ethnic-based analysis of alpha thalassaemia allelle frequency in northern Thailand.
Kulaphisit M; Kampuansai J; Leecharoenkiat K; Wathikthinnakon M; Kangwanpong D; Munkongdee T; Svasti S; Fucharoen S; Smith DR; Lithanatudom P
Sci Rep; 2017 Jul; 7(1):4690. PubMed ID: 28680061
[TBL] [Abstract][Full Text] [Related]
8. Alpha thalassaemia due to non-deletional mutations on the -3.7 alpha globin fusion gene: laboratory diagnosis and clinical importance.
Chow A; Ghassemifar R; Finlayson J
Pathology; 2013 Oct; 45(6):591-4. PubMed ID: 24018802
[TBL] [Abstract][Full Text] [Related]
9. C>A substitution in NT 46 of the 3' UTR region (the α complex protected region) of the alpha-1 globin gene: a non-deletional mutation or polymorphism?
Ropero P; González FA; Nieto JM; Villegas A; Sevilla J; Pérez G; Alonso JM; Recasens V; Abio M; Vagace JM; Vanegas RJ; González Fernández B; Martínez R
J Clin Pathol; 2020 Jan; 73(1):14-16. PubMed ID: 31434698
[TBL] [Abstract][Full Text] [Related]
10. Multi-allele DNA biosensor for the rapid genotyping of 'nondeletion' alpha thalassaemia mutations in HBA1 and HBA2 genes by means of multiplex primer extension reaction.
Petropoulou M; Poula A; Traeger-Synodinos J; Kanavakis E; Christopoulos TK; Ioannou PC
Clin Chim Acta; 2015 Jun; 446():241-7. PubMed ID: 25892676
[TBL] [Abstract][Full Text] [Related]
11. Rapid detection of non-deletional mutations causing α-thalassemia by multicolor melting curve analysis.
Huang Q; Wang X; Tang N; Zhu C; Yan T; Chen P; Li Q
Clin Chem Lab Med; 2016 Mar; 54(3):397-402. PubMed ID: 26351923
[TBL] [Abstract][Full Text] [Related]
12. Simplified PGD of common determinants of haemoglobin Bart's hydrops fetalis syndrome using multiplex-microsatellite PCR.
Wang W; Yap CH; Loh SF; Tan AS; Lim MN; Prasath EB; Chan ML; Tan WC; Jiang B; Yeo GH; Mathew J; Ho A; Ho SS; Wong PC; Choolani MA; Chong SS
Reprod Biomed Online; 2010 Nov; 21(5):642-8. PubMed ID: 20864413
[TBL] [Abstract][Full Text] [Related]
13. A multiplex qPCR gene dosage assay for rapid genotyping and large-scale population screening for deletional α-thalassemia.
Zhou W; Wang G; Zhao X; Xiong F; Zhou S; Peng J; Cheng Y; Xu S; Xu X
J Mol Diagn; 2013 Sep; 15(5):642-51. PubMed ID: 23810501
[TBL] [Abstract][Full Text] [Related]
14. Non-deletional alpha thalassaemia: a review.
Kalle Kwaifa I; Lai MI; Md Noor S
Orphanet J Rare Dis; 2020 Jun; 15(1):166. PubMed ID: 32600445
[TBL] [Abstract][Full Text] [Related]
15. Detection of alpha-thalassemia in China by using multiplex ligation-dependent probe amplification.
Liu JZ; Han H; Schouten JP; Wang LR; Fan XP; Duarte HB; Zhu CJ; Cai R; Xiao B; Wang QT
Hemoglobin; 2008; 32(6):561-71. PubMed ID: 19065334
[TBL] [Abstract][Full Text] [Related]
16. Detection of rare thalassemia mutations using long-read single-molecule real-time sequencing.
Jiang F; Mao AP; Liu YY; Liu FZ; Li YL; Li J; Zhou JY; Tang XW; Ju AP; Li FT; Wan JH; Zuo LD; Li DZ
Gene; 2022 May; 825():146438. PubMed ID: 35306112
[TBL] [Abstract][Full Text] [Related]
17. [Rapid detection of three common deletional alpha thalassemias in Chinese by single-tube multiplex PCR].
Zhou Y; Zhang Y; Li L; Li W; Mo Q; Zheng Q; Xu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Apr; 22(2):180-4. PubMed ID: 15793780
[TBL] [Abstract][Full Text] [Related]
18. Clinical validation of a single-tube PCR and reverse dot blot assay for detection of common α-thalassaemia and β-thalassaemia in Chinese.
Liang HF; Li LJ; Yang H; Zheng XB; Lu M; Ge YY; Lin F; Xie LX; Yang LY
J Int Med Res; 2022 Feb; 50(2):3000605221078785. PubMed ID: 35225055
[TBL] [Abstract][Full Text] [Related]
19. Combined use of gap-PCR and next-generation sequencing improves thalassaemia carrier screening among premarital adults in China.
Zhao J; Li J; Lai Q; Yu Y
J Clin Pathol; 2020 Aug; 73(8):488-492. PubMed ID: 31980563
[TBL] [Abstract][Full Text] [Related]
20. Molecular characteristic of alpha thalassaemia among patients diagnosed in UKM Medical Centre.
Azma RZ; Ainoon O; Hafiza A; Azlin I; Noor Farisah AR; Nor Hidayati S; Noor Hamidah H
Malays J Pathol; 2014 Apr; 36(1):27-32. PubMed ID: 24763232
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]