159 related articles for article (PubMed ID: 37330590)
21. [Application of multiplex ligation-dependent probe amplification technique in prenatal diagnosis of α-thalassemia].
Hao Y; Xu X; Xu Z; Jiang N; Wu W; Jin Q; Yin S; Cai Y; Xie J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Oct; 32(5):683-6. PubMed ID: 26418992
[TBL] [Abstract][Full Text] [Related]
22. Characterization of Hb Bart's Hydrops Fetalis Caused by - -
He S; Li J; Huang P; Zhang S; Lin L; Zuo Y; Tian X; Zheng C; Qiu X; Chen B
Hemoglobin; 2018 Jan; 42(1):61-64. PubMed ID: 29493331
[TBL] [Abstract][Full Text] [Related]
23. Molecular Characterization of Hb H and AEBart’s Diseases in Thai Children: Phramongkutklao Hospital Experiences.
Boonyawat B; Photia A; Monsereenusorn C; Rujkijyanont P; Traivaree C
J Med Assoc Thai; 2017 Feb; 100(2):167-74. PubMed ID: 29916623
[TBL] [Abstract][Full Text] [Related]
24. [Molecular screening and prenatal diagnosis of the deletional alpha-thalassemia by polymerase chain reaction amplification].
Xu XM; Cai XH; Li J
Zhonghua Yi Xue Za Zhi; 1994 Aug; 74(8):495-7, 520. PubMed ID: 7994662
[TBL] [Abstract][Full Text] [Related]
25. Invasive prenatal diagnosis of α-thalassemia to control Hb Bart's hydrops fetalis syndrome: 15 years of experience.
Lai K; Li S; Lin W; Yang D; Chen W; Li M; Pang L; Chen P
Arch Gynecol Obstet; 2018 Aug; 298(2):307-311. PubMed ID: 29948167
[TBL] [Abstract][Full Text] [Related]
26. Association of Hb A
Panyasai S; Pornprasert S
Hemoglobin; 2020 May; 44(3):179-183. PubMed ID: 32482156
[TBL] [Abstract][Full Text] [Related]
27. Molecular and hematological studies in a large cohort of α(0)-thalassemia in northeast Thailand: data from a single referral center.
Chaibunruang A; Prommetta S; Yamsri S; Fucharoen G; Sae-Ung N; Sanchaisuriya K; Fucharoen S
Blood Cells Mol Dis; 2013 Aug; 51(2):89-93. PubMed ID: 23639268
[TBL] [Abstract][Full Text] [Related]
28. The diverse molecular basis and hematological features of Hb H and AEBart's diseases in Northeast Thailand.
Boonsa S; Sanchaisuriya K; Fucharoen G; Wiangnon S; Jetsrisuparb A; Fucharoen S
Acta Haematol; 2004; 111(3):149-54. PubMed ID: 15034236
[TBL] [Abstract][Full Text] [Related]
29. Development of pre-implantation genetic testing protocol for monogenic disorders (PGT-M) of Hb H disease.
Somboonchai P; Charoenkwan P; Piyamongkol S; Lattiwongsakorn W; Pantasri T; Piyamongkol W
BMC Genomics; 2024 Jul; 25(1):668. PubMed ID: 38961367
[TBL] [Abstract][Full Text] [Related]
30. Novel α
Moore JA; Pullon BM; Drake KM; Brennan SO
Hemoglobin; 2020 Jul; 44(4):297-301. PubMed ID: 32722952
[TBL] [Abstract][Full Text] [Related]
31. Diagnosis of the accurate genotype of HKαα carriers in patients with thalassemia using multiplex ligation-dependent probe amplification combined with nested polymerase chain reaction.
Chen DM; Ma S; Tang XL; Yang JY; Yang ZL
Chin Med J (Engl); 2020 May; 133(10):1175-1181. PubMed ID: 32433049
[TBL] [Abstract][Full Text] [Related]
32. Alpha(0)-thalassemia and related disorders in northeast Thailand: a molecular and hematological characterization.
Sae-ung N; Fucharoen G; Sanchaisuriya K; Fucharoen S
Acta Haematol; 2007; 117(2):78-82. PubMed ID: 17106191
[TBL] [Abstract][Full Text] [Related]
33. Detection of alpha(0)-thalassemia South-East Asian-type deletion by droplet digital PCR.
Pornprasert S; Prasing W
Eur J Haematol; 2014 Mar; 92(3):244-8. PubMed ID: 24330258
[TBL] [Abstract][Full Text] [Related]
34. Molecular characterization of a novel 83.9-kb deletion of the α-globin upstream regulatory elements by long-read sequencing.
Feng J; Mao A; Lu Y; Shi H; Meng W; Liang C
Blood Cells Mol Dis; 2023 Nov; 103():102764. PubMed ID: 37336681
[TBL] [Abstract][Full Text] [Related]
35. Criteria for detection of alpha-thalassemia-1 Thai type deletion in routine laboratory.
Pornprasert S; Punyamung M; Treesuwan K
Clin Lab; 2013; 59(11-12):1423-7. PubMed ID: 24409681
[TBL] [Abstract][Full Text] [Related]
36. Molecular diagnosis of α-thalassemia in a multiethnic population.
Gilad O; Shemer OS; Dgany O; Krasnov T; Nevo M; Noy-Lotan S; Rabinowicz R; Amitai N; Ben-Dor S; Yaniv I; Yacobovich J; Tamary H
Eur J Haematol; 2017 Jun; 98(6):553-562. PubMed ID: 28160324
[TBL] [Abstract][Full Text] [Related]
37. Development and application of a real-time quantitative PCR for prenatal detection of fetal alpha(0)-thalassemia from maternal plasma.
Tungwiwat W; Fucharoen S; Fucharoen G; Ratanasiri T; Sanchaisuriya K
Ann N Y Acad Sci; 2006 Sep; 1075():103-7. PubMed ID: 17108198
[TBL] [Abstract][Full Text] [Related]
38. Retrospective study and implementation of a low-cost LAMP-turbidimetric assay for screening α
Jomoui W; Saknava K; Prechatrammaruch K; Ondee Y
PeerJ; 2024; 12():e17054. PubMed ID: 38436007
[TBL] [Abstract][Full Text] [Related]
39. PCR-based analysis of alpha-thalassemia in Southern Taiwan.
Chen TP; Liu TC; Chang CS; Chang JG; Tsai HJ; Lin SF
Int J Hematol; 2002 Apr; 75(3):277-80. PubMed ID: 11999355
[TBL] [Abstract][Full Text] [Related]
40. Co-inheritance of alpha-and beta-thalassemia in Khuzestan Province, Iran.
Rahim F; Kaikhaei B; Zandian K; Hoseini A
Hematology; 2008 Feb; 13(1):59-64. PubMed ID: 18534068
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
