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Journal Abstract Search

298 related items for PubMed ID: 11360286

  • 1. Alpha-thalassaemia prenatal diagnosis by two PCR-based methods.
    Kleanthous M, Kyriacou K, Kyrri A, Kalogerou E, Vassiliades P, Drousiotou A, Kallikas I, Ioannou P, Angastiniotis M.
    Prenat Diagn; 2001 May; 21(5):413-7. PubMed ID: 11360286
    [Abstract] [Full Text] [Related]

  • 2. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
    Karnpean R, Fucharoen G, Fucharoen S, Sae-ung N, Sanchaisuriya K, Ratanasiri T.
    Acta Haematol; 2009 May; 121(4):227-33. PubMed ID: 19546525
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.
    Li D, Liao C, Li J, Xie X, Huang Y, Zhong H.
    Haematologica; 2006 May; 91(5):649-51. PubMed ID: 16627247
    [Abstract] [Full Text] [Related]

  • 5. 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 May; 22(4):264-8. PubMed ID: 17369692
    [Abstract] [Full Text] [Related]

  • 6. [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
    [Abstract] [Full Text] [Related]

  • 7. 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; 26 Suppl 1():287-90. PubMed ID: 8629126
    [Abstract] [Full Text] [Related]

  • 8. Noninvasive prenatal exclusion of haemoglobin Bart's using foetal DNA from maternal plasma.
    Ho SS, Chong SS, Koay ES, Ponnusamy S, Chiu L, Chan YH, Rauff M, Baig S, Chan J, Su LL, Biswas A, Hahn S, Choolani M.
    Prenat Diagn; 2010 Jan; 30(1):65-73. PubMed ID: 19960446
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis of Hb Bart's hydrops fetalis in West Malaysia: the identification of the alpha thal 1 defect by PCR based strategies.
    George E, Mokhtar AB, Azman ZA, Hasnida K, Saripah S, Hwang CM.
    Singapore Med J; 1996 Oct; 37(5):501-4. PubMed ID: 9046203
    [Abstract] [Full Text] [Related]

  • 10. Rapid and cost-effective antenatal diagnosis of haemoglobin Bart's hydrops foetalis syndrome using a duplex-polymerase chain reaction.
    Wee YC, Tan KL, Tan PC, Yap SF, Tan JA.
    Med J Malaysia; 2005 Oct; 60(4):447-53. PubMed ID: 16570706
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of hemoglobin Bart's hydrops fetalis by HPLC analysis of hemoglobin in fetal blood samples.
    Sanguansermsri T, Thanaratanakorn P, Steger HF, Tongsong T, Sirivatanapa P, Wanapirak C, Sirichotiyakul S, Chanprapas P, Flatz G.
    Southeast Asian J Trop Med Public Health; 2001 Mar; 32(1):180-5. PubMed ID: 11485083
    [Abstract] [Full Text] [Related]

  • 12. Rapid prenatal diagnosis of Hb Bart's hydrops fetalis in southeast Asia area by polymerase chain reaction.
    Chang JG, Chen CP, Ho HJ, Lin CP, Lee LS, Chen PH.
    Int J Hematol; 1992 Oct; 56(2):155-9. PubMed ID: 1421177
    [Abstract] [Full Text] [Related]

  • 13. Prevention of beta-thalassemia major and Hb Bart's hydrops fetalis syndrome.
    Beris P, Darbellay R, Extermann P.
    Semin Hematol; 1995 Oct; 32(4):244-61. PubMed ID: 8560282
    [No Abstract] [Full Text] [Related]

  • 14. α-Thalassemia with Haemoglobin Adana mutation: prenatal diagnosis.
    Zainal NZ, Alauddin H, Ahmad S, Hussin NH.
    Malays J Pathol; 2014 Dec; 36(3):207-11. PubMed ID: 25500521
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis of hemoglobin Bart's hydrops fetalis with gap-PCR system.
    Li DZ.
    Acta Haematol; 2009 Dec; 122(1):50; author reply 51. PubMed ID: 19816007
    [No Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. Prenatal diagnosis of alpha-thalassemia-1 (SEA type) by chorionic villus sampling.
    Chanprapaph P, Tongsong T, Wanapirak C, Sirichotiyakul S, Sanguansermsri T.
    J Med Assoc Thai; 2002 Oct; 85(10):1049-53. PubMed ID: 12501894
    [Abstract] [Full Text] [Related]

  • 18. Non-radioactive Southern hybridization for early diagnosis of alpha-thalassemia with southeast Asian-type deletion in Taiwan.
    Chu DC, Lee CH, Lo MD, Cheng SW, Chen DP, Wu TL, Tsao KC, Chiu DT, Sun CF.
    Am J Med Genet; 2000 Dec 11; 95(4):332-5. PubMed ID: 11186886
    [Abstract] [Full Text] [Related]

  • 19. The molecular basis of alpha-thalassemia in Thailand.
    Winichagoon P, Fucharoen S, Wasi P.
    Southeast Asian J Trop Med Public Health; 1992 Dec 11; 23 Suppl 2():7-13. PubMed ID: 1298997
    [Abstract] [Full Text] [Related]

  • 20. [Genetic screening for alpha-thalassemia deletional determinants by GapPCR method].
    Katol J, Takao M, Ideguchi H, Sawada H, Kawashima H, Ono J.
    Rinsho Byori; 2006 Nov 11; 54(11):1095-100. PubMed ID: 17240829
    [Abstract] [Full Text] [Related]

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