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Journal Abstract Search

373 related items for PubMed ID: 27373361

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  • 2. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N, Pinmuang-Ngam C, Fucharoen G, Fucharoen S.
    Fetal Diagn Ther; 2007; 22(4):264-8. PubMed ID: 17369692
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  • 4. Analysis of real-time PCR cycle threshold of alpha-thalassemia-1 Southeast Asian type deletion using fetal cell-free DNA in maternal plasma for noninvasive prenatal diagnosis of Bart's hydrops fetalis.
    Pornprasert S, Sukunthamala K, Kunyanone N, Sittiprasert S, Thungkham K, Junorse S, Pongsawatkul K, Pattanaporn W, Jitwong C, Sanguansermsri T.
    J Med Assoc Thai; 2010 Nov; 93(11):1243-8. PubMed ID: 21114201
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  • 5. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS, He J, Zhang J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
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  • 6. Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (- -SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart's Hydrops Fetalis Syndrome in Thailand.
    Jomoui W, Tepakhan W, Karnpean R.
    Hemoglobin; 2019 Feb; 43(4-5):236-240. PubMed ID: 31635494
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  • 8. 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
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  • 10. Genetic origin of α0-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart's hydrops fetalis syndrome.
    Jomoui W, Fucharoen G, Sanchaisuriya K, Charoenwijitkul P, Maneesarn J, Xu X, Fucharoen S.
    J Hum Genet; 2017 Aug; 62(8):747-754. PubMed ID: 28381876
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  • 11. Diagnostic value of fetal hemoglobin Bart's for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy.
    Singha K, Yamsri S, Chaibunruang A, Srivorakun H, Sanchaisuriya K, Fucharoen G, Fucharoen S.
    Orphanet J Rare Dis; 2022 Feb 10; 17(1):45. PubMed ID: 35144630
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  • 14. 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 10; 298(2):307-311. PubMed ID: 29948167
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  • 15. Comparison of red blood cell hematology among normal, alpha-thalassemia-1 trait, and hemoglobin Bart's fetuses at mid-pregnancy.
    Srisupundit K, Piyamongkol W, Tongsong T.
    Am J Hematol; 2008 Dec 10; 83(12):908-10. PubMed ID: 18932192
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  • 16. The molecular basis of alpha-thalassemia in Thailand.
    Winichagoon P, Fucharoen S, Wasi P.
    Southeast Asian J Trop Med Public Health; 1992 Dec 10; 23 Suppl 2():7-13. PubMed ID: 1298997
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  • 19. Noninvasive prenatal detection of hemoglobin Bart hydrops fetalis via maternal plasma dispensed with parental haplotyping using the semiconductor sequencing platform.
    Yang J, Peng CF, Qi Y, Rao XQ, Guo F, Hou Y, He W, Wu J, Chen YY, Zhao X, Wang YN, Peng H, Wang D, Du L, Luo MY, Huang QF, Liu HL, Yin A.
    Am J Obstet Gynecol; 2020 Feb 10; 222(2):185.e1-185.e17. PubMed ID: 31394068
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  • 20. Prenatal diagnosis of Hb Bart's hydrops fetalis by PCR technique: Pramongkutklao experience.
    Torcharus K, Sriphaisal T, Krutvecho T, Ketupanya A, Vuthiwong C, Suwanasophon C, Noonai A.
    Southeast Asian J Trop Med Public Health; 1995 Feb 10; 26 Suppl 1():287-90. PubMed ID: 8629126
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