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PUBMED FOR HANDHELDS

Journal Abstract Search


157 related items for PubMed ID: 8895695

  • 1. Prenatal diagnosis based on simultaneous DNA analysis for alpha- and beta-globin genes.
    Oron-Karni V, Filon D, Rund D, Rachmilewitz E, Oppenheim A.
    Am J Hematol; 1996 Nov; 53(3):203-4. PubMed ID: 8895695
    [No Abstract] [Full Text] [Related]

  • 2. Molecular genetics and prenatal diagnosis of the thalassaemias.
    Thein SL.
    Malays J Pathol; 1997 Jun; 19(1):1-9. PubMed ID: 10879235
    [No Abstract] [Full Text] [Related]

  • 3. Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia.
    Ma ES, Chan AY, Au WY, Yeung YM, Chan LC.
    Haematologica; 2001 Apr; 86(4):432-3. PubMed ID: 11325652
    [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. Alpha and beta thalassemias in Hong Kong.
    Chan V, Chan TK, Todd D.
    Chin Med J (Engl); 1997 Jun; 110(6):490-3. PubMed ID: 9594254
    [No Abstract] [Full Text] [Related]

  • 6. [A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].
    Li Q, Li LY, Mo QH.
    Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jan; 28(1):16-9. PubMed ID: 18227017
    [Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis of unusual hemoglobinopathies.
    Kim JH, Lebo RV, Cai SP, Su X, Chung JH, Mentzer WC, Golbus MS.
    Am J Med Genet; 1994 Mar 01; 50(1):15-20. PubMed ID: 8160747
    [Abstract] [Full Text] [Related]

  • 8. [Genetic diagnosis of alpha and beta thalassemia dual heterozygote].
    Zeng R, Yu S, Hu B.
    Zhonghua Xue Ye Xue Za Zhi; 1998 Oct 01; 19(10):525-7. PubMed ID: 11189497
    [Abstract] [Full Text] [Related]

  • 9. Simultaneous detection of alpha-thalassemia and beta-thalassemia by oligonucleotide microarray.
    Bang-Ce Y, Hongqiong L, Zhuanfong Z, Zhengsong L, Jianling G.
    Haematologica; 2004 Aug 01; 89(8):1010-2. PubMed ID: 15339687
    [Abstract] [Full Text] [Related]

  • 10. Prevention of beta-thalassemia major and Hb Bart's hydrops fetalis syndrome.
    Beris P, Darbellay R, Extermann P.
    Semin Hematol; 1995 Oct 01; 32(4):244-61. PubMed ID: 8560282
    [No Abstract] [Full Text] [Related]

  • 11. Detection and molecular analysis of alpha and beta thalassaemia genes--recent developments in screening protocols.
    Tan J, Tay JS, Wong HB.
    J Singapore Paediatr Soc; 1992 Oct 01; 34(1-2):53-6. PubMed ID: 1303468
    [Abstract] [Full Text] [Related]

  • 12. [Accurate and rapid prenatal diagnosis of beta-thalassemia by a multiplex primer extension and denaturing high-performance liquid chromatography technique].
    Hua L, Zhu H, Li XR, Li J, Mo QH, Liao C, Hou YX, Zhong M, Xu XM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec 01; 21(6):600-3. PubMed ID: 15583991
    [Abstract] [Full Text] [Related]

  • 13. Simultaneous PCR detection of beta - thalassemia and alpha - thalassemia 1 (SEA type) in prenatal diagnosis of complex thalassemia syndrome.
    Siriratmanawong N, Fucharoen G, Sanchaisuriya K, Ratanasiri T, Fucharoen S.
    Clin Biochem; 2001 Jul 01; 34(5):377-80. PubMed ID: 11522274
    [Abstract] [Full Text] [Related]

  • 14. Feasibility of prenatal diagnosis of beta-thalassemia using two highly polymorphic microsatellites 5' to the beta-globin gene.
    Loudianos G, Cao A, Pirastu M.
    Haematologica; 1992 Jul 01; 77(4):361-2. PubMed ID: 1427447
    [Abstract] [Full Text] [Related]

  • 15. Unusual phenotype of hemoglobin EE with hemoglobin H disease: a pitfall in clinical diagnosis and genetic counseling.
    Viprakasit V, Tanphaichitr VS.
    J Pediatr; 2004 Mar 01; 144(3):391-3. PubMed ID: 15001953
    [Abstract] [Full Text] [Related]

  • 16. 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 Mar 01; 121(4):227-33. PubMed ID: 19546525
    [Abstract] [Full Text] [Related]

  • 17. [Diagnosis of several common alpha-thalassemia genotypes by multiplex fluorescence polymerase chain reaction].
    Wen S, Wu LQ, Li Q.
    Hunan Yi Ke Da Xue Xue Bao; 2003 Apr 01; 28(2):123-6. PubMed ID: 12934354
    [Abstract] [Full Text] [Related]

  • 18. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
    Srivorakun H, Fucharoen G, Sae-Ung N, Sanchaisuriya K, Ratanasiri T, Fucharoen S.
    Eur J Haematol; 2009 Jul 01; 83(1):57-65. PubMed ID: 19226360
    [Abstract] [Full Text] [Related]

  • 19. Mild hemoglobin H-constant spring disease with β-thalassemia-a case report.
    Li DZ, Liao C, Zhou JY, Xie XM, Li J.
    Ann Hematol; 2011 Jan 01; 90(1):123-4. PubMed ID: 20383502
    [No Abstract] [Full Text] [Related]

  • 20. Non-invasive first-trimester detection of paternal beta-globin gene mutations and polymorphisms as predictors of thalassemia risk at chorionic villous sampling.
    Lazaros L, Hatzi E, Bouba I, Makrydimas G, Dalkalitsis N, Stefos T, Paraskevaidis E, Georgiou I.
    Eur J Obstet Gynecol Reprod Biol; 2008 Sep 01; 140(1):17-20. PubMed ID: 18353524
    [Abstract] [Full Text] [Related]


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