These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

299 related items for PubMed ID: 9061749

  • 1. Haemoglobinopathies.
    Old J.
    Prenat Diagn; 1996 Dec; 16(13):1181-6. PubMed ID: 9061749
    [Abstract] [Full Text] [Related]

  • 2. Screening and genetic diagnosis of haemoglobinopathies.
    Old JM.
    Scand J Clin Lab Invest; 2007 Dec; 67(1):71-86. PubMed ID: 17365985
    [Abstract] [Full Text] [Related]

  • 3. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China.
    Xiong F, Sun M, Zhang X, Cai R, Zhou Y, Lou J, Zeng L, Sun Q, Xiao Q, Shang X, Wei X, Zhang T, Chen P, Xu X.
    Clin Genet; 2010 Aug; 78(2):139-48. PubMed ID: 20412082
    [Abstract] [Full Text] [Related]

  • 4. Screening and genetic diagnosis of haemoglobin disorders.
    Old JM.
    Blood Rev; 2003 Mar; 17(1):43-53. PubMed ID: 12490210
    [Abstract] [Full Text] [Related]

  • 5. Prenatal diagnosis of inherited hemoglobinopathies.
    Cao A, Rosatelli C, Pirastu M.
    J Genet Hum; 1986 Nov; 34(5):413-24. PubMed ID: 3540210
    [Abstract] [Full Text] [Related]

  • 6. Molecular biologic diagnosis of the hemoglobinopathies.
    Schwartz E, Surrey S.
    Hosp Pract (Off Ed); 1986 Sep 15; 21(9):163-78. PubMed ID: 3091617
    [No Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis of beta-thalassaemia mutations using the reverse dot blot technique.
    Muralitharan S, Srivastava A, Shaji RV, Mathai M, Srivastava VM, Dennison D, Lu CY, Krishnamoorthy R.
    Natl Med J India; 1996 Sep 15; 9(2):70-1. PubMed ID: 8857041
    [Abstract] [Full Text] [Related]

  • 8. Molecular diagnosis of haemoglobin disorders.
    Clark BE, Thein SL.
    Clin Lab Haematol; 2004 Jun 15; 26(3):159-76. PubMed ID: 15163314
    [Abstract] [Full Text] [Related]

  • 9. A pilot beta-thalassaemia screening program in the Albanian population for a health planning program.
    Baghernajad-Salehi L, D'Apice MR, Babameto-Laku A, Biancolella M, Mitre A, Russo S, Di Daniele N, Sangiuolo F, Mokini V, Novelli G.
    Acta Haematol; 2009 Jun 15; 121(4):234-8. PubMed ID: 19556751
    [Abstract] [Full Text] [Related]

  • 10. Carrier screening and prenatal diagnosis of hemoglobinopathies. A study of indigenous and immigrant couples in northern Greece, over the last 5 years.
    Theodoridou S, Alemayehou M, Prappas N, Karakasidou O, Aletra V, Plata E, Tsaftaridis P, Karababa P, Boussiou M, Sinopoulou K, Hatzi A, Voskaridou E, Loutradi A, Manitsa A.
    Hemoglobin; 2008 Jun 15; 32(5):434-9. PubMed ID: 18932067
    [Abstract] [Full Text] [Related]

  • 11. [Prenatal diagnosis of hereditary hemoglobinopathies].
    Cao A, Pirastu M, Rosatelli C.
    Haematologica; 1989 Oct 15; 74(5 Suppl):213-22. PubMed ID: 2574134
    [No Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis of haemoglobinopathies.
    Arora S, Kabra M, Maheshwari M, Shastri S, Kaur D, Deka D, Kriplani A, Menon PS.
    Natl Med J India; 2001 Oct 15; 14(6):340-2. PubMed ID: 11804364
    [Abstract] [Full Text] [Related]

  • 13. The intrauterine diagnosis of hemoglobin disorders.
    Wong SC, Ali MA, Benzie R.
    Clin Perinatol; 1984 Jun 15; 11(2):283-308. PubMed ID: 6086205
    [Abstract] [Full Text] [Related]

  • 14. 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 Jun 15; 121(4):227-33. PubMed ID: 19546525
    [Abstract] [Full Text] [Related]

  • 15. Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies.
    Patrinos GP, Kollia P, Papadakis MN.
    Hum Mutat; 2005 Nov 15; 26(5):399-412. PubMed ID: 16138310
    [Abstract] [Full Text] [Related]

  • 16. Preventation of thalassemia in Australia.
    Hendy J.
    Southeast Asian J Trop Med Public Health; 1999 Nov 15; 30 Suppl 2():94-6. PubMed ID: 11400797
    [Abstract] [Full Text] [Related]

  • 17. Control and prevention of the genetic load of haemoglobinopathies in India.
    Balgir RS.
    Natl Med J India; 1999 Nov 15; 12(5):234-8. PubMed ID: 10613007
    [Abstract] [Full Text] [Related]

  • 18. [Gene diagnosis of hemoglobinopathies--the determination of breakpoints for a large deletion].
    Hattori Y, Yamashiro Y.
    Rinsho Byori; 2003 Jun 15; 51(6):550-5. PubMed ID: 12884742
    [Abstract] [Full Text] [Related]

  • 19. [Prenatal diagnosis of hemoglobinopathies in the 1st and 2nd pregnancy trimesters].
    Ferrari M, Cantù Rajnoldi A, Cremonesi L, Donzelli C, Pietri S, Tedeschi S, Travi M, Nicolini U, Brambati B.
    Pediatr Med Chir; 1984 Jun 15; 6(6):769-73. PubMed ID: 6545587
    [Abstract] [Full Text] [Related]

  • 20. [Diagnosis of hemoglobinopathies and thalassemias].
    Brosstad F, Stavem P, Kofstad J, Gran T.
    Tidsskr Nor Laegeforen; 1993 Sep 30; 113(23):2925-8. PubMed ID: 8236198
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.