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Journal Abstract Search

374 related items for PubMed ID: 19556751

  • 21. Frequency of haemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in Basra.
    Hassan MK, Taha JY, Al-Naama LM, Widad NM, Jasim SN.
    East Mediterr Health J; 2003; 9(1-2):45-54. PubMed ID: 15562732
    [Abstract] [Full Text] [Related]

  • 22. Characterisation of beta-globin gene mutations in Malaysian children: a strategy for the control of beta-thalassaemia in a developing country.
    Thong MK, Tan JA, Tan KL, Yap SF.
    J Trop Pediatr; 2005 Dec; 51(6):328-33. PubMed ID: 15967770
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  • 23. 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 Dec; 9(2):70-1. PubMed ID: 8857041
    [Abstract] [Full Text] [Related]

  • 24. Molecular genetics of beta-thalassaemia syndrome in Pakistan.
    Usman M, Moinuddin M, Ghani R.
    East Mediterr Health J; 2010 Sep; 16(9):972-6. PubMed ID: 21218725
    [Abstract] [Full Text] [Related]

  • 25. Neonatal haemoglobinopathy screening in Belgium.
    Gulbis B, Cotton F, Ferster A, Ketelslegers O, Dresse MF, Rongé-Collard E, Minon JM, Lé PQ, Vertongen F.
    J Clin Pathol; 2009 Jan; 62(1):49-52. PubMed ID: 19103861
    [Abstract] [Full Text] [Related]

  • 26. Starting neonatal screening for haemoglobinopathies in The Netherlands.
    Giordano PC.
    J Clin Pathol; 2009 Jan; 62(1):18-21. PubMed ID: 19103852
    [Abstract] [Full Text] [Related]

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

  • 28. Delta-thalassemia in Cyprus.
    Pavlou E, Phylactides M, Kyrri A, Kalogerou E, Makariou C, Georgiou I, Kleanthous M.
    Hemoglobin; 2006 Dec; 30(4):455-62. PubMed ID: 16987800
    [Abstract] [Full Text] [Related]

  • 29. [Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].
    Fattoum S.
    Tunis Med; 2006 Nov; 84(11):687-96. PubMed ID: 17294892
    [Abstract] [Full Text] [Related]

  • 30. [Hemoglobinopathy in the county of Copenhagen].
    Birgens HS, Karle H, Guldberg P, Güttler F.
    Ugeskr Laeger; 1997 Jun 16; 159(25):3934-9. PubMed ID: 9214066
    [Abstract] [Full Text] [Related]

  • 31. The spectrum of haemoglobin variants in two scheduled tribes of Sundargarh district in north-western Orissa, India.
    Balgir RS.
    Ann Hum Biol; 2005 Jun 16; 32(5):560-73. PubMed ID: 16316913
    [Abstract] [Full Text] [Related]

  • 32. Molecular basis of haemoglobinopathies and G6PD deficiency in the Comorian population.
    Badens C, Martinez di Montemuros F, Thuret I, Michel G, Mattei JF, Cappellini MD, Lena-Russo D.
    Hematol J; 2000 Jun 16; 1(4):264-8. PubMed ID: 11920200
    [Abstract] [Full Text] [Related]

  • 33. The molecular heterogeneity of beta-thalassemia in Greece.
    Boussiou M, Karababa P, Sinopoulou K, Tsaftaridis P, Plata E, Loutradi-Anagnostou A.
    Blood Cells Mol Dis; 2008 Jun 16; 40(3):317-9. PubMed ID: 18096416
    [Abstract] [Full Text] [Related]

  • 34. Thirty-year experience in preventing haemoglobinopathies in Greece: achievements and potentials for optimisation.
    Ladis V, Karagiorga-Lagana M, Tsatra I, Chouliaras G.
    Eur J Haematol; 2013 Apr 16; 90(4):313-22. PubMed ID: 23331260
    [Abstract] [Full Text] [Related]

  • 35. Quantitation of beta-thalassemia genes in Quebec immigrants of Mediterranean, southeast Asian, and Asian Indian origins.
    Kaplan F, Kokotsis G, Capua A, Scriver CR.
    Clin Invest Med; 1991 Aug 16; 14(4):325-30. PubMed ID: 1782730
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  • 36. Genetic heterogeneity of Beta thalassemia in Lebanon reflects historic and recent population migration.
    Makhoul NJ, Wells RS, Kaspar H, Shbaklo H, Taher A, Chakar N, Zalloua PA.
    Ann Hum Genet; 2005 Jan 16; 69(Pt 1):55-66. PubMed ID: 15638828
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  • 37. Rapid detection of beta-Thalassemia alleles in Egypt using naturally or amplified created restriction sites and direct sequencing: a step in disease control.
    Hussein G, Fawzy M, Serafi TE, Ismail EF, Metwally DE, Saber MA, Giansily M, Schved JF, Pissard S, Martinez PA.
    Hemoglobin; 2007 Jan 16; 31(1):49-62. PubMed ID: 17365005
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  • 38. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN.
    Hemoglobin; 2007 Jan 16; 31(2):233-41. PubMed ID: 17486506
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  • 39. Screening of concurrent alpha-thalassaemia 1 in beta-thalassaemia carriers.
    Chong YM, Tan JA, Zubaidah Z, Rahimah A, Kuldip K, George E.
    Med J Malaysia; 2006 Jun 16; 61(2):217-20. PubMed ID: 16898315
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  • 40. Sickle cell anemia, sickle cell beta-thalassemia, and thalassemia major in Albania: characterization of mutations.
    Boletini E, Svobodova M, Divoky V, Baysal E, Cürük MA, Dimovski AJ, Liang R, Adekile AD, Huisman TH.
    Hum Genet; 1994 Feb 16; 93(2):182-7. PubMed ID: 8112743
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