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344 related items for PubMed ID: 16466950

  • 1. Prevalence of -alpha(3.7) and alpha alpha alpha(anti3.7) alleles in sickle cell trait and beta-thalassemia patients in Mexico.
    Nava MP, Ibarra B, Magaña MT, de la Luz Chávez M, Perea FJ.
    Blood Cells Mol Dis; 2006; 36(2):255-8. PubMed ID: 16466950
    [Abstract] [Full Text] [Related]

  • 2. Triplication (/alphaalphaalpha anti3.7) or deletion (-alpha3.7/) association in Argentinian beta-thalassemic carriers.
    Bragós IM, Noguera NI, Raviola MP, Milani AC.
    Ann Hematol; 2003 Nov; 82(11):696-8. PubMed ID: 13680176
    [Abstract] [Full Text] [Related]

  • 3. Molecular heterogeneity of beta-thalassemia alleles in Spain and its importance in the diagnosis and prevention of beta-thalassemia major and sickle cell disorders.
    Pereira Mdel M, Dalmau AC, Corrons JL.
    Hemoglobin; 2009 Nov; 33(3):226-34. PubMed ID: 19657837
    [Abstract] [Full Text] [Related]

  • 4. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM, El-Khatib FF, Ayesh S.
    Hemoglobin; 2005 Nov; 29(2):119-32. PubMed ID: 15921164
    [Abstract] [Full Text] [Related]

  • 5. [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]

  • 6. Segmental duplications involving the alpha-globin gene cluster are causing beta-thalassemia intermedia phenotypes in beta-thalassemia heterozygous patients.
    Harteveld CL, Refaldi C, Cassinerio E, Cappellini MD, Giordano PC.
    Blood Cells Mol Dis; 2008 Nov; 40(3):312-6. PubMed ID: 18249014
    [Abstract] [Full Text] [Related]

  • 7. Molecular characterization of beta-thalassemia mutations in Guadeloupe.
    Romana M, Keclard L, Guillemin G, Lavocat E, Saint-Martin C, Berchel C, Mérault G.
    Am J Hematol; 1996 Dec; 53(4):228-33. PubMed ID: 8948659
    [Abstract] [Full Text] [Related]

  • 8. [Molecular diagnosis of beta-thalassemia intermedia].
    Chen J, Liu W, Chen M.
    Zhonghua Yi Xue Za Zhi; 1997 Aug; 77(8):575-8. PubMed ID: 9772460
    [Abstract] [Full Text] [Related]

  • 9. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
    Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK.
    Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
    [Abstract] [Full Text] [Related]

  • 10. Molecular characterization of sickle cell anemia in the Northern Brazilian state of Pará.
    De Lemos Cardoso G, Guerreiro JF.
    Am J Hum Biol; 2010 Nov; 22(5):573-7. PubMed ID: 20737602
    [Abstract] [Full Text] [Related]

  • 11. Spectrum of beta-thalassemia mutations in North Indian states: a beta-thalassemia trait with two mutations in cis.
    Chakrabarti P, Gupta R, Mishra A, Rai M, Singh VP, Dash D.
    Clin Biochem; 2005 Jun; 38(6):576-8. PubMed ID: 15885239
    [Abstract] [Full Text] [Related]

  • 12. [The prevalence of beta-thalassemia heterozygotes compound alpha-thalassemia in Guangdong district].
    Han J, Zeng R, Hu B.
    Zhonghua Xue Ye Xue Za Zhi; 2001 Oct; 22(10):514-6. PubMed ID: 11769674
    [Abstract] [Full Text] [Related]

  • 13. Molecular epidemiological study of alpha- and beta-thalassemia in Sihui city.
    Tan JR, Li WJ, Ma JY, Mo QH, Li LY, Jia SQ, Lao XW, Li LY, He RQ, Xu XM.
    Di Yi Jun Yi Da Xue Xue Bao; 2003 Jul; 23(7):716-9. PubMed ID: 12865230
    [Abstract] [Full Text] [Related]

  • 14. [Prevalence survey and molecular characterization of alpha and beta thalassemia in Liuzhou city of Guangxi].
    Cai R, Li L, Liang X, Liu Z, Su L, Li W, Zhu Q, Mo Q, Pan L, Ouyang H, Huang L, Xu X.
    Zhonghua Liu Xing Bing Xue Za Zhi; 2002 Aug; 23(4):281-5. PubMed ID: 12411074
    [Abstract] [Full Text] [Related]

  • 15. [Molecular genetics of the thalassemias in Argentina].
    Varela V, Rossetti LC, Binaghi A, Targovnik HM, Abreu MS.
    Sangre (Barc); 1999 Jun; 44(3):210-5. PubMed ID: 10481583
    [Abstract] [Full Text] [Related]

  • 16. Evidence of differential selection for the -α(3.7) and -α(4.2) single-α-globin gene deletions within the same population.
    Yap ZM, Sun KM, Teo CR, Tan AS, Chong SS.
    Eur J Haematol; 2013 Mar; 90(3):210-3. PubMed ID: 23289742
    [Abstract] [Full Text] [Related]

  • 17. [Thalassemic alleles in Mexican mestizos].
    Ibarra B, Perea FJ, Villalobos-Arámbula AR.
    Rev Invest Clin; 1995 Mar; 47(2):127-31. PubMed ID: 7610281
    [Abstract] [Full Text] [Related]

  • 18. Molecular analysis of beta-thalassemia and sickle cell anemia in Antalya.
    Keser I, Sanlioglu AD, Manguoglu E, Guzeloglu Kayisli O, Nal N, Sargin F, Yesilipek A, Simsek M, Mendilcioglu I, Canatan D, Luleci G.
    Acta Haematol; 2004 Mar; 111(4):205-10. PubMed ID: 15153712
    [Abstract] [Full Text] [Related]

  • 19. The carrier frequency of α-globin gene triplication in an Iranian population with normal or borderline hematological parameters.
    Moosavi SF, Amirian A, Zarbakhsh B, Kordafshari A, Mirzahoseini H, Zeinali S, Karimipoor M.
    Hemoglobin; 2011 Mar; 35(4):323-30. PubMed ID: 21797699
    [Abstract] [Full Text] [Related]

  • 20. Analysis of beta-thalassemia mutations and beta-locus control region hypersensitive sites 2, 3 and 4 in southern Thailand.
    Sriroongrueng W, Schleiemacher E, Panich V, Nopparatana C, Saechan V, Laosombat V, Pornpatkul M, Fukumaki Y.
    Southeast Asian J Trop Med Public Health; 1997 Mar; 28 Suppl 3():120-7. PubMed ID: 9640613
    [Abstract] [Full Text] [Related]


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