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Journal Abstract Search

277 related items for PubMed ID: 9046203

  • 21. 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]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. [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 10; 74(8):495-7, 520. PubMed ID: 7994662
    [Abstract] [Full Text] [Related]

  • 24. 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 10; 1075():103-7. PubMed ID: 17108198
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. 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 Dec 10; 43(4-5):236-240. PubMed ID: 31635494
    [Abstract] [Full Text] [Related]

  • 27. Prenatal diagnosis of thalassemia and hemoglobinopathies in Thailand: experience from 100 pregnancies.
    Fucharoen S, Winichagoon P, Thonglairoam V, Siriboon W, Siritanaratkul N, Kanokpongsakdi S, Vantanasiri C.
    Southeast Asian J Trop Med Public Health; 1991 Mar 10; 22(1):16-29. PubMed ID: 1948258
    [Abstract] [Full Text] [Related]

  • 28. Noninvasive prenatal diagnosis for hemoglobin Bart's hydrops fetalis.
    Winichagoon P, Sithongdee S, Kanokpongsakdi S, Tantisirin P, Bernini LF, Fucharoen S.
    Int J Hematol; 2005 Jun 10; 81(5):396-9. PubMed ID: 16158819
    [Abstract] [Full Text] [Related]

  • 29. Analysis of Deletional Hb H Diseases in Samples with Hb A2-Hb H and Hb A2-Hb Bart's on Capillary Electrophoresis.
    Khongthai K, Ruengdit C, Panyasai S, Pornprasert S.
    Hemoglobin; 2019 Jun 10; 43(4-5):245-248. PubMed ID: 31687860
    [Abstract] [Full Text] [Related]

  • 30. Electrophoresis features and genotypes of Hb bart's hydrops fetalis.
    Li Y, Liang L, Tian M, Qing T, Wu X.
    Scand J Clin Lab Invest; 2020 Jun 10; 80(2):129-132. PubMed ID: 31841045
    [Abstract] [Full Text] [Related]

  • 31. [Incidental diagnosis of homozygous alpha-zero thalassemia in a 21 week old fetus].
    Legras B, Lucas-Clerc C, Doualin G, Audiau C, Ruelland A, Vialard J, Cloarec L.
    Pathol Biol (Paris); 1991 Jan 10; 39(1):50-3. PubMed ID: 2011411
    [Abstract] [Full Text] [Related]

  • 32. [Major alpha-thalassemia: antenatal diagnosis, case report and literature review].
    Saadi H, Alexander S, Barlow P, Van Regemorter N, Gulbis B, Thomas D.
    J Gynecol Obstet Biol Reprod (Paris); 2009 May 10; 38(3):258-62. PubMed ID: 19303226
    [Abstract] [Full Text] [Related]

  • 33. 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 10; 30(1):65-73. PubMed ID: 19960446
    [Abstract] [Full Text] [Related]

  • 34. Prenatal diagnosis of homozygous alpha-thalassemia-1 by cell-free fetal DNA in maternal plasma.
    Sirichotiyakul S, Charoenkwan P, Sanguansermsri T.
    Prenat Diagn; 2012 Jan 10; 32(1):45-9. PubMed ID: 22031039
    [Abstract] [Full Text] [Related]

  • 35. Prevention of beta-thalassemia major and Hb Bart's hydrops fetalis syndrome.
    Beris P, Darbellay R, Extermann P.
    Semin Hematol; 1995 Oct 10; 32(4):244-61. PubMed ID: 8560282
    [No Abstract] [Full Text] [Related]

  • 36. Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome.
    Chen M, Chan JK, Nadarajah S, Tan AS, Chan ML, Mathew J, Saw EE, Lim C, Wong W, Cheah FS, Law HY, Wong PC, Chong SS.
    Prenat Diagn; 2015 Jun 10; 35(6):534-43. PubMed ID: 25641621
    [Abstract] [Full Text] [Related]

  • 37. Detection of alpha-thalassemia-1 (Southeast Asian type) and its application for prenatal diagnosis.
    Winichagoon P, Fucharoen S, Kanokpongsakdi S, Fukumaki Y.
    Clin Genet; 1995 Jun 10; 47(6):318-20. PubMed ID: 7554366
    [Abstract] [Full Text] [Related]

  • 38. Analysis of real-time SYBR-polymerase chain reaction cycle threshold for diagnosis of the alpha-thalassemia-1 Southeast Asian type deletion: application to carrier screening and prenatal diagnosis of Hb Bart's hydrops fetalis.
    Pornprasert S, Sukunthamala K, Sacome J, Phusua A, Saetung R, Sanguansermsri T, Leechanachai P.
    Hemoglobin; 2008 Jun 10; 32(4):393-402. PubMed ID: 18654890
    [Abstract] [Full Text] [Related]

  • 39. [Prenatal diagnosis of Thailand deletion of alpha-thalassemia 1].
    Chen P, Li SQ, Li MQ, Pang LH, Lin WX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun 10; 24(3):247-50. PubMed ID: 17557230
    [Abstract] [Full Text] [Related]

  • 40. Hb Bart's Hydrops Fetalis Syndrome and Hb H Disease Caused by Deletional Chiang Rai (- -CR) α0-Thalassemia in Two Unrelated Thai Families.
    Ruengdit C, Khamphikham P, Jinorose N, Pornprasert S.
    Hemoglobin; 2021 Mar 10; 45(2):75-79. PubMed ID: 33821735
    [Abstract] [Full Text] [Related]

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