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Journal Abstract Search

320 related items for PubMed ID: 8112743

  • 1. 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; 93(2):182-7. PubMed ID: 8112743
    [Abstract] [Full Text] [Related]

  • 2. Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among Tunisians.
    Fattoum S, Guemira F, Oner C, Oner R, Li HW, Kutlar F, Huisman TH.
    Hemoglobin; 1991 Feb; 15(1-2):11-21. PubMed ID: 1917531
    [Abstract] [Full Text] [Related]

  • 3. Sickle cell disease in the Kurdish population of northern Iraq.
    Al-Allawi NA, Jalal SD, Nerwey FF, Al-Sayan GO, Al-Zebari SS, Alshingaly AA, Markous RD, Jubrael JM, Hamamy H.
    Hemoglobin; 2012 Feb; 36(4):333-42. PubMed ID: 22686351
    [Abstract] [Full Text] [Related]

  • 4. Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics.
    Belisário AR, Carneiro-Proietti AB, Sabino EC, Araújo A, Loureiro P, Máximo C, Flor-Park MV, Rodrigues DDOW, Ozahata MC, McClure C, Mota RA, Gomes Moura IC, Custer B, Kelly S, Recipient Epidemiology and Donor Evaluation Study (REDS-III) International Component Brazil.
    Hemoglobin; 2020 Jan; 44(1):1-9. PubMed ID: 32172616
    [Abstract] [Full Text] [Related]

  • 5. Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs.
    Adekile AD, Gu LH, Baysal E, Haider MZ, al-Fuzae L, Aboobacker KC, al-Rashied A, Huisman TH.
    Acta Haematol; 1994 Jan; 92(4):176-81. PubMed ID: 7701914
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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 Dec; 111(4):205-10. PubMed ID: 15153712
    [Abstract] [Full Text] [Related]

  • 8. The beta+-IVS-I-6 (T-->C) mutation accounts for half of the thalassemia chromosomes in the Palestinian populations of the mountain regions.
    El-Latif MA, Filon D, Rund D, Oppenheim A, Kanaan M.
    Hemoglobin; 2002 Feb; 26(1):33-40. PubMed ID: 11939510
    [Abstract] [Full Text] [Related]

  • 9. Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.
    Murad H, Moassas F, Jarjour R, Mukhalalaty Y, Al-Achkar W.
    Hemoglobin; 2014 Feb; 38(6):390-3. PubMed ID: 25405916
    [Abstract] [Full Text] [Related]

  • 10. Frequencies and phenotypic consequences of association of α- and β-thalassemia alleles with sickle-cell disease in Bahrain.
    Abuamer S, Shome DK, Jaradat A, Radhi A, Bapat JP, Sharif KA, Al-Touq J, Al-Asheeri A, Al-Ajami A.
    Int J Lab Hematol; 2017 Feb; 39(1):76-83. PubMed ID: 27981798
    [Abstract] [Full Text] [Related]

  • 11. Phenotype and genotype frequency of β-thalassemia and sickle cell disease carriers in Halkidiki, Northern Greece.
    Kalleas C, Anagnostopoulos K, Sinopoulou K, Delaki E, Margaritis D, Bourikas G, Tsatalas C, Kortsaris A, Tentes I.
    Hemoglobin; 2012 Feb; 36(1):64-72. PubMed ID: 22188117
    [Abstract] [Full Text] [Related]

  • 12. Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemia.
    Schiliro G, Samperi P, Testa R, Gupta RB, Gu LH, Huisman TH.
    Am J Hematol; 1992 Dec; 41(4):264-9. PubMed ID: 1283809
    [Abstract] [Full Text] [Related]

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

  • 14. Molecular basis of beta-thalassemia in the Maldives.
    Furuumi H, Firdous N, Inoue T, Ohta H, Winichagoon P, Fucharoen S, Fukumaki Y.
    Hemoglobin; 1998 Mar; 22(2):141-51. PubMed ID: 9576331
    [Abstract] [Full Text] [Related]

  • 15. Unusual β-Globin Haplotype Distribution in Newborns from Bengo, Angola.
    Borges E, Tchonhi C, Couto CSB, Gomes V, Amorim A, Prata MJ, Brito M.
    Hemoglobin; 2019 May; 43(3):149-154. PubMed ID: 31394941
    [Abstract] [Full Text] [Related]

  • 16. 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 May; 29(2):119-32. PubMed ID: 15921164
    [Abstract] [Full Text] [Related]

  • 17. Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.
    Jha AN, Mishra H, Verma HK, Pandey I, Lakkakula BVKS.
    Hemoglobin; 2018 Mar; 42(2):84-90. PubMed ID: 30200838
    [Abstract] [Full Text] [Related]

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  • 20. Sickle Cell Disease in Jordan: The Experience of a Major Referral Center.
    Oudat RI, Abualruz HS, Al-Shiek NKA, Al-Mashaqba EA, Al-Hiari RA, Alsoukhni HA, Hammad MAA.
    Med Arch; 2021 Feb; 75(1):27-30. PubMed ID: 34012195
    [Abstract] [Full Text] [Related]

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